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Camila Norethindrone .35 mg Tablet, 84-count — NDC 75907-0074-32 package photo
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Camila Norethindrone .35 mg Tablet, 84-count — NDC 75907-074-32 (Billing 75907-0074-32)

by Dr. Reddy's Labratories Inc. · 3 BLISTER PACK in 1 CARTON / 28 TABLET in 1 BLISTER PACK

This is a package of 84 tablets of Camila Norethindrone .35 mg Tablet from Dr. Reddy's Labratories Inc., marketed since May 2024 and currently FDA-listed; retail pharmacies pay about $0.0924 per tablet (NADAC). It is this product's only package size.

NDC 75907-0074-32
🏷️ FDA NDC (as labeled) 75907-074-32 billing pads the product segment with a zero
Rx only Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 75907-074-32
Product NDC 75907-074
11-digit billing NDC 75907007432
NCPDP billing unit EA — each (per item)
RxCUI 198042, 748961, 748962
UNII T18F433X4S
Application # ANDA076177
SPL Set ID 59985565-af09-21ba-0336-3f6db7711bd1
Established class (EPC) Progestin
Chemical class Progesterone Congeners
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-05-06
Route ORAL
Dosage form TABLET
Substance NORETHINDRONE
TE code (Orange Book) AB1 · RLD · RS

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GPI-14 25100010000305
GCN Seq No 003313
GCN 11520
HICL code 001459
Ingredient (HICL) Norethindrone
HIC1 code G
Therapeutic class — broad (HIC1) Female Genital System
HIC2 code G8
Therapeutic class — intermediate (HIC2) Systemic Antifertility Agents
HIC3 code G8A
Therapeutic class — specific (HIC3) Contraceptives,Oral
AHFS code 68:12.00.00
AHFS class Contraceptives
FDB label name CAMILA 0.35 MG TABLET
FDB brand name Camila
Legend status F — Federal legend — prescription drug or device
Quick answers
  • GSN (GCN sequence number): 003313
  • GCN: 11520
  • GPI-14 (Medi-Span): 25100010000305
  • HICL (First Databank): 001459
  • AHFS class code: 68:12.00.00
  • RxCUI (RxNorm): 198042
Why two NDCs? The FDA registers this code as 75907-074-32 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 75907-0074-32. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Progestin class.

Pharmacologic class Progestin
Drug family (ATC) Progestogens and estrogens, sequential preparations, Progestogens, Estren derivatives
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

Label name CAMILA 0.35 MG TABLET Ingredient Norethindrone
📗 Our plain-language guide HelloPharmacist
  • Most norethindrone products, like Errin, Camila and Emzahh, are progestin-only birth control pills that prevent pregnancy. Norethindrone acetate tablets, such as Gallifrey, are use...
  • Take one tablet by mouth every day at the same time. Don't take a break between packs. Following the schedule exactly gives you the best protection, so follow your label and the pa...
  • Changes in your bleeding are the most common, including irregular or frequent bleeding. Some people get headache, breast tenderness, nausea or dizziness. Call me or your doctor if...
  • It's best not to. Smoking greatly raises the risk of heart attack and stroke in women using oral contraceptives. If you smoke, let's talk about options and quitting.
📖 Read our full Norethindrone guide →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eaPer package
Retail pharmacies payNADAC · weekly $0.092 $7.76 / 84 tablets
Medicaid paysCMS SDUD · 12 mo $0.2550 $21.42 / 84 tablets
Medicare drug plans payPart D · Q2 2026 $0.1895 $15.92 / 84 tablets
NADAC price history (per ea) — tap or hover for the price & month
Dec 2025 Mar 2026 Jun 2026 Sep 2026 $0.095 $0.085
▲ Up 9% over the last 10 months.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
75907-0074-32 You're viewing this Main listing 3 BLISTER PACK in 1 CARTON / 28 TABLET in 1 BLISTER PACK 2024-05-06 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Camila .35 mg 51862-0884-03 Mayne 84 tablets $0.091 AB1 Discontinued save 2%
Errin .35 mg 51862-0886-03 Mayne 84 tablets $0.091 AB2 Discontinued save 2%
Norethindrone .35 mg 00378-7292-53 Mylan 84 tablets $0.091 AB1 Availability likely save 2%
Incassia .35 mg 65862-0925-28 Aurobindo 1 tablet $0.092 AB1 Availability likely —
Lyleq .35 mg 50102-0300-13 Afaxys 84 tablets $0.092 AB1 Availability likely —
Emzahh .35 mg 59651-0136-28 Aurobindo 1 tablet $0.092 AB2 Availability likely —
Meleya .35 mg 70700-0317-85 Xiromed 84 tablets $0.092 AB2 Availability likely —
Norethindrone .35 mg 68462-0305-29 Glenmark 84 tablets $0.092 AB2 Availability likely —
Orquidea .35 mg 70700-0316-85 Xiromed, 84 tablets $0.092 AB1 Availability likely —
Camila .35 mgthis 75907-0074-32 Dr. 84 tablets $0.092 AB1 Availability likely —
Norethindrone .35 mg 68180-0876-73 Lupin 84 tablets $0.092 AB1 Availability likely —
Jencycla .35 mg 68180-0877-73 Lupin 28 tablets $0.092 AB2 Availability likely —
Heather .35 mg 68462-0303-29 Glenmark 84 tablets $0.092 AB1 Availability likely —
Nora BE .35 mg 00480-3475-16 Teva 168 tablets $0.092 AB1 Availability likely —
Errin .35 mg 75907-0075-32 Dr. 84 tablets $0.092 AB2 Availability likely —
Nora BE .35 mg 52544-0629-28 Actavis 168 tablets $0.094 AB1 Discontinued +2%
Norethindrone .35 mg 63187-0748-28 Proficient 28 tablets — AB2 FDA listed —
Errin .35 mg 71205-0526-28 Proficient 28 tablets — AB2 FDA listed —
Norethindrone .35 mg 60505-4900-08 Apotex 84 tablets — AB1 FDA listed —
Affodel .35 mg 79929-0015-07 Naari 2352 tablets — AB1 FDA listed —
Norethindrone .35 mg 82804-0175-28 Proficient 28 tablets — AB1 FDA listed —
Norethindrone .35 mg 50090-6161-00 A-S 28 tablets — AB1 FDA listed —
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2024
On the market since
May 2024
📍
2026
Currently FDA-listed
2 years listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerDr. Reddy's Labratories Inc.
Application holderDR REDDYS LABORATORIES SA
FDA applicationANDA076177 (ANDA)
Labeler code75907
First marketedMay 2024
Product typeHuman Prescription Drug
Portfolio32 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

Full prescribing information FDA SPL

The complete FDA label for this product — the official prescribing information, verbatim, section by section. Very long sections are excerpted here and marked; the full text is on DailyMed (linked in the sources below). Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ~3 min read ▾

INDICATIONS AND USAGE 1. Indications Progestin-only oral contraceptives are indicated for the prevention of pregnancy. 2.

Efficacy If used perfectly, the first-year failure rate for progestin-only oral contraceptives is 0.5%. However, the typical failure rate is estimated to be closer to 5%, due to late or omitted pills. The following table lists the pregnancy rates for users of all major methods of contraception.

Table 2: Percentage of Women Experiencing an Unintended Pregnancy During the First Year of Typical Use and the First Year of Perfect Use of Contraception and the Percentage Continuing Use at the End of the First Year. United States. % of Women Experiencing an Unintended Pregnancy within the First Year of Use % of Women Continuing Use at One Year Method (1) Typical Use Among typical couples who initiate use of a method (not necessarily for the first time), the percentage who experience an accidental pregnancy during the first year if they do not stop use for any reason.

(2) Perfect Use Among couples who initiate use of a method (not necessarily for the first time), and who use it perfectly (both consistently and correctly), the percentage who experience an accidental pregnancy during the first year if they do not stop use for any other reason. (3) (4) Emergency Contraceptive Pills: Treatment initiated within 72 hours after unprotected intercourse reduces the risk of pregnancy by at least 75%. The treatment schedule is one dose within 72 hours after unprotected intercourse, and a second dose 12 hours after the first dose.

The Food and Drug Administration has declared the following brands of oral contraceptives to be safe and effective for emergency contraception: Ovral (1 dose is 2 white pills), Alesse (1 dose is 5 pink pills), Nordette or Levlen (1 dose is 4 yellow pills). Lactational Amenorrhea Method: LAM is a highly effective, temporary method of contraception. However, to maintain effective protection against pregnancy, another method of contraception must be used as soon as menstruation resumes, the frequency or duration of breastfeeds is reduced, bottle feeds are introduced, or the baby reaches 6 months of age.

Source: Trussell, J, Contraceptive Efficacy. In: Hatcher RA, Trussell J, Stewart F, Cates W, Stewart GK, Kowal D, Guest F, Contraceptive Technology: Seventeenth Revised Edition. New York NY: Irvington Publishers, 1998.

3 Among couples attempting to avoid pregnancy, the percentage who continue to use a method for one year. Chance The percentage of women becoming pregnant noted in columns (2) and (3) are based on data from populations where contraception is not used and from women who cease using contraception in order to become pregnant. Among such populations, about 89% become pregnant within one year.

This estimate was lowered slightly (to 85%) to represent the percentage that would become pregnant within one year among women now relying on reversible methods of contraception if they abandoned contraception altogether. 85 85 Spermicides Foams, creams, gels, vaginal suppositories, and vaginal film. 26 6 40 Periodic Abstinence Calendar Ovulation Method Sympto-Thermal Cervical mucus (ovulation) method supplemented by calendar in the pre-ovulatory and basal body temperature in the post-ovulatory phases.

Post-Ovulation 25 9 3 2 1 63 Cap With spermicidal cream or jelly. Parous Women 40 26 42 Nulliparous Women 20 9 56 Sponge Parous Women 40 20 42 Nulliparous Women 20 9 56 Diaphragm 20 6 56 Withdrawal 19 4 Condom Without spermicides. Female (Reality) 21 5 56 Male 14 3 61 Pill 5 71 Progestin-only

0.5 Combined

0.1IUDs Progesterone T 2 1.5 81 Copper T380A 0.8 0.6 78 LNg 20 0.1 0.1 81 Depo-Provera 0.3 0.3 70 Levonorgestrel Implants (Norplant) 0.05 0.05 88 Female Sterilization 0.5 0.5 100 Male Sterilization 0.15 0.10 100

⏱️ Dosage and Administration 40 words ▾

DOSAGE AND ADMINISTRATION To achieve maximum contraceptive effectiveness, Camila must be taken exactly as directed. One tablet is taken every day, at the same time. Administration is continuous, with no interruption between pill packs. See PATIENT LABELING for detailed instructions.

⛔ Contraindications 47 words ▾

CONTRAINDICATIONS Progestin-only oral contraceptives (POPs) should not be used by women who currently have the following conditions: Known or suspected pregnancy Known or suspected carcinoma of the breast Undiagnosed abnormal genital bleeding Hypersensitivity to any component of this product Benign or malignant liver tumors Acute liver disease

⚠️ Warnings ~3 min read ▾

WARNINGS Cigarette smoking greatly increases the possibility of suffering heart attacks and strokes. Women who use oral contraceptives are strongly advised not to smoke. Camila does not contain estrogen and, therefore, this insert does not discuss the serious health risks that have been associated with the estrogen component of combined oral contraceptives.

The health care provider is referred to the prescribing information of combined oral contraceptives for a discussion of those risks, including, but not limited to, an increased risk of serious cardiovascular disease in women who smoke, carcinoma of the breast and reproductive organs, hepatic neoplasia, and changes in carbohydrate and lipid metabolism. The relationship between progestin-only oral contraceptives and these risks have not been established and there are no studies definitely linking progestin-only pill (POP) use to an increased risk of heart attack or stroke.

The physician should remain alert to the earliest manifestation of symptoms of any serious disease and discontinue oral contraceptive therapy when appropriate. 1. Ectopic Pregnancy The incidence of ectopic pregnancies for progestin-only oral contraceptive users is 5 per 1000 woman-years.

Up to 10% of pregnancies reported in clinical studies of progestin-only oral contraceptive users are extrauterine. Although symptoms of ectopic pregnancy should be watched for, a history of ectopic pregnancy need not be considered a contraindication to use of this contraceptive method. Health providers should be alert to the possibility of an ectopic pregnancy in women who become pregnant or complain of lower abdominal pain while on progestin-only oral contraceptives.

2. Delayed Follicular Atresia/Ovarian Cysts If follicular development occurs, atresia of the follicle is sometimes delayed, and the follicle may continue to grow beyond the size it would attain in a normal cycle. Generally these enlarged follicles disappear spontaneously.

Often they are asymptomatic; in some cases they are associated with mild abdominal pain. Rarely they may twist or rupture, requiring surgical intervention. 3.

Irregular Genital Bleeding Irregular menstrual patterns are common among women using progestin-only oral contraceptives. If genital bleeding is suggestive of infection, malignancy or other abnormal conditions, such nonpharmacologic causes should be ruled out. If prolonged amenorrhea occurs, the possibility of pregnancy should be evaluated.

4. Carcinoma of the Breast and Reproductive Organs Some epidemiologic studies of oral contraceptive users have reported an increased relative risk of developing breast cancer, particularly at a younger age and apparently related to duration of use. These studies have predominantly involved combined oral contraceptives and there is insufficient data to determine whether the use of POPs similarly increase the risk.

Women with breast cancer should not use oral contraceptives because the role of female hormone in breast cancer has not been fully determined. Some studies suggest that oral contraceptive use has been associated with an increase in the risk of cervical intraepithelial neoplasia in some populations of women. However, there continues to be controversy about the extent to which such findings may be due to differences in sexual behavior and other factors.

There is insufficient data to determine whether the use of POPs increases the risk of developing cervical intraepithelial neoplasia. 5. Hepatic Neoplasia Benign hepatic adenomas are associated with combined oral contraceptive use, although the incidence of benign tumors is rare in the United States.

Rupture of benign, hepatic adenomas may cause death through intraabdominal hemorrhage. Studies from Britain and the U.S. have shown an increased risk of developing hepatocellular carcinoma in combined oral contraceptive users. However, these cancers are rare.

There is insufficient data to determine whether POPs increase the risk of developing hepatic… [Excerpted — this section continues on DailyMed.]

🤒 Adverse Reactions 80 words ▾

ADVERSE REACTIONS Menstrual irregularity is the most frequently reported side effect. Frequent and irregular bleeding are common, while long duration of bleeding episodes and amenorrhea are less likely. Headache, breast tenderness, nausea, and dizziness are increased among progestin-only oral contraceptive users in some studies.

Androgenic side effects such as acne, hirsutism, and weight gain occur rarely. To report SUSPECTED ADVERSE EVENTS, contact Dr. Reddy’s Laboratories Inc, at 1-888-375-3784 or FDA at 1-800-FDA-1088 or http://www.fda.gov/medwatch for voluntary reporting of adverse reactions.

🔄 Drug Interactions 171 words ▾

4. Drug Interactions Change in contraceptive effectiveness associated with coadministration of other products: a. Anti-infective Agents and Anticonvulsants Contraceptive effectiveness may be reduced when hormonal contraceptives are coadministered with antibiotics, anticonvulsants, and other drugs that increase the metabolism of contraceptive steroids.

This could result in unintended pregnancy or breakthrough bleeding. Examples include rifampin, barbiturates, phenylbutazone, phenytoin, carbamazepine, felbamate, oxcarbazepine, topiramate, and griseofulvin. b. Anti-HIV Protease Inhibitors Several of the anti-HIV protease inhibitors have been studied with coadministration of oral contraceptives; significant changes (increase and decrease) in the plasma levels of the estrogen and progestin have been noted in some cases.

The safety and efficacy of OC products may be affected with the coadministration of anti-HIV protease inhibitors. Health care providers should refer to the label of the individual anti-HIV protease inhibitors for further drug-drug interaction information. c. Herbal Products Herbal products containing St.

John's Wort (hypericum perforatum) may induce hepatic enzymes (cytochrome P450) and p-glycoprotein transporter and may reduce the effectiveness of contraceptive steroids. This may also result in breakthrough bleeding.

🔄 Drug / Laboratory Test Interactions 39 words ▾

5. Interactions With Laboratory Tests The following endocrine tests may be affected by progestin-only oral contraceptive use: Sex hormone-binding globulin (SHBG) concentrations may be decreased. Thyroxine concentrations may be decreased, due to a decrease in thyroid binding globulin (TBG).

🤰 Pregnancy 54 words ▾

7. Pregnancy Many studies have found no effects on fetal development associated with long-term use of contraceptive doses of oral progestins. The few studies of infant growth and development that have been conducted have not demonstrated significant adverse effects. It is nonetheless prudent to rule out suspected pregnancy before initiating any hormonal contraceptive use.

🧒 Pediatric Use 49 words ▾

12. Pediatric Use Safety and efficacy of Camila have been established in women of reproductive age. Safety and efficacy are expected to be the same for postpubertal adolescents under the age of 16 and for users 16 years and older. Use of this product before menarche is not indicated.

🆘 Overdosage 16 words ▾

OVERDOSAGE There have been no reports of serious ill effects from overdosage, including ingestion by children.

🧬 Clinical Pharmacology ~2 min read ▾

CLINICAL PHARMACOLOGY 1. Mode of Action Camila progestin-only oral contraceptives prevent conception by suppressing ovulation in approximately half of users, thickening the cervical mucus to inhibit sperm penetration, lowering the mid-cycle LH and FSH peaks, slowing the movement of the ovum through the fallopian tubes, and altering the endometrium. 2.

Pharmacokinetics Absorption Norethindrone is rapidly absorbed with maximum plasma concentrations occurring within 1 to 2 hours after Camila administration (see Table 1 ). Norethindrone appears to be completely absorbed following oral administration; however, it is subject to first pass metabolism resulting in an absolute bioavailability of approximately 65%. Figure 1: Mean ± SD Norethindrone Plasma Concentrations Following Camila Administration.

Peak plasma concentrations occur approximately 1 hour after administration (mean T max 1.2 hours). The mean (SD) C max was 4816.8 (1532.6) pg/mL and generally occurred within 1 hour (mean) of tablet administration, ranging from 0.5 to 2 hours. The mean (SD) C avg was 885 (250) pg/mL, however, the mean concentration at 24 hrs was 130 (47) pg/mL.

Table 1 provides summary statistics of the pharmacokinetic parameters associated with single dose Camila administration. Table 1: Mean ± SD Pharmacokinetic Parameters Following Single Dose Administration of Camila in 12 Healthy Female Subjects Under Fasting Conditions Pharmacokinetic Parameter Norethindrone 0.35 mg T max (hr) 1.2 ±

0.05C max (pg/mL) 4817 ± 1533 AUC (0-48) (pg∙h/mL) 21233 ± 6002 t 1/2 (h) 7.7 ±

0.5The food effect on the rate and extent of norethindrone absorption after Camila administration has not been evaluated. Distribution Following oral administration, norethindrone is 36% bound to sex hormone-binding globulin (SHBG) and 61% bound to albumin. Volume of distribution of norethindrone is approximately 4 L/kg.

Metabolism Norethindrone undergoes extensive biotransformation, primarily via reduction, followed by sulfate and glucuronide conjugation; less than 5% of a norethindrone dose is excreted unchanged; greater than 50% and 20 to 40% of a dose is excreted in urine and feces, respectively. The majority of metabolites in the circulation are sulfate, with glucuronides accounting for most of the urinary metabolites. Excretion Plasma clearance rate for norethindrone has been estimated to be approximately 600 L/day.

Norethindrone is excreted in both urine and feces, primarily as metabolites. The mean terminal elimination half-life of norethindrone following single dose administration of Camila is approximately 8 hours.

🧬 Mechanism of Action 47 words ▾

1. Mode of Action Camila progestin-only oral contraceptives prevent conception by suppressing ovulation in approximately half of users, thickening the cervical mucus to inhibit sperm penetration, lowering the mid-cycle LH and FSH peaks, slowing the movement of the ovum through the fallopian tubes, and altering the endometrium.

📦 How Supplied / Storage and Handling 69 words ▾

HOW SUPPLIED Camila ® (norethindrone tablets USP, 0.35 mg) are packaged in cartons of 3 blister cards (NDC 75907-074-32) each containing 28 tablets. Each light pink, round, flat-faced, beveled-edge, unscored tablet is debossed with m on one side and 884 on the other side. KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN. STORAGE Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature].

📦 Storage and Handling 14 words ▾

STORAGE Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature].

📋 Description 62 words ▾

DESCRIPTION Each light pink Camila® tablet provides a continuous oral contraceptive regimen of 0.35 mg norethindrone, USP daily, and has the following inactive ingredients: corn starch, FD&C red no. 40 aluminum lake, lactose monohydrate, magnesium stearate, povidone and sodium starch glycolate. The chemical name for norethindrone is 17-Hydroxy-19-nor-17α-pregn-4-en-20-yn-3-one.

The structural formula follows: Therapeutic class = oral contraceptive. Meets USP Dissolution Test 2.

💬 Information for Patients 122 words ▾

INFORMATION FOR THE PATIENT See PATIENT LABELING for detailed information. Counseling Issues The following points should be discussed with prospective users before prescribing progestin-only oral contraceptives: The necessity of taking pills at the same time every day, including throughout all bleeding episodes. The need to use a backup method such as condoms and spermicides for the next 48 hours whenever a progestin-only oral contraceptive is taken 3 or more hours late.

The potential side effects of progestin-only oral contraceptives, particularly menstrual irregularities. The need to inform the clinician of prolonged episodes of bleeding, amenorrhea or severe abdominal pain. The importance of using a barrier method in addition to progestin-only oral contraceptives if a woman is at risk of contracting or transmitting STDs/HIV.

⚠️ Precautions ~3 min read ▾

PRECAUTIONS 1. General Patients should be counseled that oral contraceptives do not protect against transmission of HIV (AIDS) and other sexually transmitted diseases (STDs) such as Chlamydia, genital herpes, genital warts, gonorrhea, hepatitis B, and syphilis. 2.

Physical Examination and Follow-up It is considered good medical practice for sexually active women using oral contraceptives to have annual history and physical examinations. The physical examination may be deferred until after initiation of oral contraceptives if requested by the woman and judged appropriate by the clinician. 3.

Carbohydrate and Lipid Metabolism Some users may experience slight deterioration in glucose tolerance, with increases in plasma insulin, but women with diabetes mellitus who use progestin-only oral contraceptives do not generally experience changes in their insulin requirements. Nonetheless, prediabetic and diabetic women in particular should be carefully monitored while taking POPs. Lipid metabolism is occasionally affected in that HDL, HDL2, and apolipoprotein A-I and A-II may be decreased; hepatic lipase may be increased.

There is no effect on total cholesterol, HDL3, LDL, or VLDL. 4. Drug Interactions Change in contraceptive effectiveness associated with coadministration of other products: a.

Anti-infective Agents and Anticonvulsants Contraceptive effectiveness may be reduced when hormonal contraceptives are coadministered with antibiotics, anticonvulsants, and other drugs that increase the metabolism of contraceptive steroids. This could result in unintended pregnancy or breakthrough bleeding. Examples include rifampin, barbiturates, phenylbutazone, phenytoin, carbamazepine, felbamate, oxcarbazepine, topiramate, and griseofulvin. b.

Anti-HIV Protease Inhibitors Several of the anti-HIV protease inhibitors have been studied with coadministration of oral contraceptives; significant changes (increase and decrease) in the plasma levels of the estrogen and progestin have been noted in some cases. The safety and efficacy of OC products may be affected with the coadministration of anti-HIV protease inhibitors. Health care providers should refer to the label of the individual anti-HIV protease inhibitors for further drug-drug interaction information. c.

Herbal Products Herbal products containing St. John's Wort (hypericum perforatum) may induce hepatic enzymes (cytochrome P450) and p-glycoprotein transporter and may reduce the effectiveness of contraceptive steroids. This may also result in breakthrough bleeding.

5. Interactions With Laboratory Tests The following endocrine tests may be affected by progestin-only oral contraceptive use: Sex hormone-binding globulin (SHBG) concentrations may be decreased. Thyroxine concentrations may be decreased, due to a decrease in thyroid binding globulin (TBG).

6. Carcinogenesis See WARNINGS section. 7.

Pregnancy Many studies have found no effects on fetal development associated with long-term use of contraceptive doses of oral progestins. The few studies of infant growth and development that have been conducted have not demonstrated significant adverse effects. It is nonetheless prudent to rule out suspected pregnancy before initiating any hormonal contraceptive use.

8. Nursing Mothers Small amounts of progestin pass into the breast milk, resulting in steroid levels in infant plasma of 1 to 6% of the levels of maternal plasma. 6 However, isolated post-market cases of decreased milk production have been reported in POPs.

Very rarely, adverse effects in the infant/child have been reported, including jaundice. 9. Fertility Following Discontinuation The limited available data indicate a rapid return of normal ovulation and fertility following discontinuation of progestin-only oral contraceptives.

10. Headache/Migraine If you have a headache or a worsening migraine headache with a new pattern that is recurrent, persistent, or severe, this requires discontinuation of oral contraceptives and evaluation of the cau… [Excerpted — this section continues on DailyMed.]

🍼 Nursing Mothers 55 words ▾

8. Nursing Mothers Small amounts of progestin pass into the breast milk, resulting in steroid levels in infant plasma of 1 to 6% of the levels of maternal plasma. 6 However, isolated post-market cases of decreased milk production have been reported in POPs. Very rarely, adverse effects in the infant/child have been reported, including jaundice.

🧬 Pharmacokinetics ~2 min read ▾

2. Pharmacokinetics Absorption Norethindrone is rapidly absorbed with maximum plasma concentrations occurring within 1 to 2 hours after Camila administration (see Table 1 ). Norethindrone appears to be completely absorbed following oral administration; however, it is subject to first pass metabolism resulting in an absolute bioavailability of approximately 65%.

Figure 1: Mean ± SD Norethindrone Plasma Concentrations Following Camila Administration. Peak plasma concentrations occur approximately 1 hour after administration (mean T max 1.2 hours). The mean (SD) C max was 4816.8 (1532.6) pg/mL and generally occurred within 1 hour (mean) of tablet administration, ranging from 0.5 to 2 hours.

The mean (SD) C avg was 885 (250) pg/mL, however, the mean concentration at 24 hrs was 130 (47) pg/mL. Table 1 provides summary statistics of the pharmacokinetic parameters associated with single dose Camila administration. Table 1: Mean ± SD Pharmacokinetic Parameters Following Single Dose Administration of Camila in 12 Healthy Female Subjects Under Fasting Conditions Pharmacokinetic Parameter Norethindrone 0.35 mg T max (hr) 1.2 ±

0.05C max (pg/mL) 4817 ± 1533 AUC (0-48) (pg∙h/mL) 21233 ± 6002 t 1/2 (h) 7.7 ±

0.5The food effect on the rate and extent of norethindrone absorption after Camila administration has not been evaluated. Distribution Following oral administration, norethindrone is 36% bound to sex hormone-binding globulin (SHBG) and 61% bound to albumin. Volume of distribution of norethindrone is approximately 4 L/kg.

Metabolism Norethindrone undergoes extensive biotransformation, primarily via reduction, followed by sulfate and glucuronide conjugation; less than 5% of a norethindrone dose is excreted unchanged; greater than 50% and 20 to 40% of a dose is excreted in urine and feces, respectively. The majority of metabolites in the circulation are sulfate, with glucuronides accounting for most of the urinary metabolites. Excretion Plasma clearance rate for norethindrone has been estimated to be approximately 600 L/day.

Norethindrone is excreted in both urine and feces, primarily as metabolites. The mean terminal elimination half-life of norethindrone following single dose administration of Camila is approximately 8 hours.

📄 Carcinogenesis, Mutagenesis, Impairment of Fertility 5 words ▾

6. Carcinogenesis See WARNINGS section.

📄 Patient Package Insert ~3 min read ▾

DETAILED INFORMATION FOR THE PATIENT Patients should be counseled that oral contraceptives do not protect against transmission of HIV (AIDS) and other sexually transmitted diseases (STDs) such as Chlamydia, genital herpes, genital warts, gonorrhea, hepatitis B, and syphilis. INTRODUCTION This leaflet is about birth control pills that contain one hormone, a progestin. Please read this leaflet before you begin to take your pills.

It is meant to be used along with talking with your doctor or clinic. Progestin-only pills are often called "POPs" or "the minipill." POPs have less progestin than the combined birth control pill (or "the pill") which contains both an estrogen and a progestin. HOW EFFECTIVE ARE POPS?

About 1 in 200 (0.5%) POPs users will get pregnant in the first year if they all take POPs perfectly (that is, on time, every day). About 1 in 20 (5%) "typical" POPs users (including women who are late taking pills or miss pills) gets pregnant in the first year of use. The following table will help you compare the efficacy of different methods.

IUD: 1 to 2% Depo-Provera (injectable progesterone): 0.3% Norplant System (levonorgestrel implants): 0.1% Diaphragm with spermicides: 18% Spermicides alone: 21% Male condom alone: 12% Female condom alone: 21% Cervical cap: Women who have never given birth: 18% Women who have given birth: 36% Periodic abstinence: 20% No methods: 85% HOW DO POPS WORK? They make the cervical mucus at the entrance to the womb (the uterus) too thick for the sperm to get through to the egg. They prevent ovulation (release of the egg from the ovary) in about half the time.

They also affect other hormones, the fallopian tubes and the lining of the uterus. YOU SHOULD NOT TAKE POPS If there is any chance you may be pregnant. If you have breast cancer.

If you have bleeding between your periods which has not been diagnosed. If you are taking certain drugs for epilepsy (seizures) or for TB. (See USING POPS WITH OTHER MEDICINES below.) If you are hypersensitive or allergic to any component of this product.

If you have liver tumors, either benign or cancerous. If you have acute liver disease. RISKS OF TAKING POPS WARNING: If you have sudden or severe pain in your lower abdomen or stomach area, you may have an ectopic pregnancy or an ovarian cyst.

If this happens, you should contact your doctor or clinic immediately. 1. Ectopic Pregnancy An ectopic pregnancy is a pregnancy outside the womb.

Because POPs protect against pregnancy, the chance of having pregnancy outside the womb is very low. If you do get pregnant while taking POPs, you have a slightly higher chance that the pregnancy will be ectopic than do users of some other birth control methods. 2.

Ovarian Cysts These cysts are small sacs of fluid in the ovary. They are more common among POP users than among users of most other birth control methods. They usually disappear without treatment and rarely cause problems.

3. Cancer of the Reproductive Organs and Breasts Some studies in women who use combined oral contraceptives that contain both estrogen and a progestin have reported an increase in the risk of developing breast cancer, particularly at a younger age and apparently related to duration of use. There is insufficient data to determine whether the use of POPs similarly increases this risk.

Some studies have found an increase in the incidence of cancer of the cervix in women who use oral contraceptives. However, this finding may be related to factors other than the use of oral contraceptives and there is insufficient data to determine whether the use of POPs increases the risk of developing cancer of the cervix. 4.

Liver Tumors In rare cases, combined oral contraceptives can cause benign but dangerous liver tumors. These benign liver tumors can rupture and cause fatal internal bleeding. In addition, a possible but not definite association has been found with combined oral contraceptives and liver cancers in studies in which a few women who developed these ve… [Excerpted — this section continues on DailyMed.]

📖 Instructions for Use ~1 min read ▾

INSTRUCTIONS TO PATIENTS How to Use the Camila Tablets Blister Card 1. The first time you use these pills, take your first pill on the first day of your menstrual period. Pick the Days of the Week Sticker that starts the first day of your period.

When you have picked the right sticker, throw away the others and place the sticker on the blister card over the pre-printed days of the week and make sure it lines up with the pills. 2. Your blister package consists of three parts, the foil pouch, wallet, and a blister card containing 28 individually sealed pills.

Note that the pills are arranged in four numbered rows of 7 pills, with the preprinted days of the week printed above them. All 28 pills are "active" birth control pills. Refer to the sample of the blister card below: 3.

To remove a pill, push down on the pill with your thumb and forefinger so that the pill releases through the back of the blister card. Each day, take one pill. Always go from left to right along the row.

Each new row will begin on the same day of the week. 4. Take one pill every day for 28 days, whether bleeding or not, until you have taken all the pills.

It is important that you take your pill at the same time every day. 5. After you have taken all 28 pills, begin taking your pills again the next day.

Be sure that the calendar day on your new package corresponds with the actual day. All brand names listed are the registered trademarks of their respective owners and are not trademarks of Dr. Reddy’s Laboratories Inc.

Distributed by: Dr. Reddy’s Laboratories Inc. Princeton, NJ 08540 Manufactured by: Piramal Healthcare UK Limited Whalton Road Morpeth, NE61 3 YA Rev.

11/2023 20769462

📄 Package Label / Principal Display Panel 31 words ▾

PRINCIPAL DISPLAY PANEL - 0.35 mg Tablet Blister Pack Carton NDC 75907-074-32 Camila ® Norethindrone Tablets USP 0.35 mg Rx only 3 Blister Cards, 28 Tablets Each Dr. Reddy’s Laboratories Inc.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Medicaid utilization & spend

📍 This exact package only: Medicaid data is reported per full 11-digit NDC — labeler, product and pack size — so every number here is for this package alone, not the drug overall. Other pack sizes report separately.
💊 Pharmacy benefit only: These are Medicaid outpatient pharmacy claims, billed by NDC. They exclude the medical benefit — clinic- or hospital-administered drugs billed under HCPCS J-codes — so drugs used mostly that way (e.g. Avastin, Lucentis, Keytruda) can look low or missing here. That’s expected, not an error.
📅 Q1 2025 – Q1 2026 · 5 quarters of data
ⓘ The newest quarter is usually incomplete when first published; states restate recent quarters in later CMS releases, so the latest figures typically revise upward. State coverage-policy changes can also shift quarter-to-quarter totals.
Prescriptions last 4 qtrs
1.6K
Units reimbursed last 4 qtrs
76.5K
Gross reimbursed last 4 qtrs
$19.5K
Avg / prescription
$12.45
Avg / unit
$0.2550
Latest quarter Q1 2026
327Rx
Medicaid pays / ea
$0.2550
gross reimbursed
vs
NADAC / ea
$0.0924
acquisition cost
=
Spread
+$0.1626
+176% vs cost
What Medicaid paid per ea (before rebates; includes the pharmacy’s dispensing fee) compared with NADAC — the average price pharmacies pay to buy the drug. A positive spread means Medicaid reimbursed more than the purchase price, before manufacturer rebates.
Fee-for-service vs managed care ⓘ
40% FFS 60% MCO
Fee-for-service · 633 Rx Managed care · 934 Rx
State Medicaid map
Alaska: no data reported AK Maine: no data reported ME Washington: no data reported WA Idaho: no data reported ID Montana: no data reported MT North Dakota: no data reported ND Minnesota: no data reported MN Wisconsin: 952 units · 16.1 per 100k residents WI Michigan: 3,808 units · 37.9 per 100k residents MI New York: 18,824 units · 96.2 per 100k residents NY Vermont: no data reported VT New Hampshire: no data reported NH Oregon: no data reported OR Nevada: no data reported NV Wyoming: no data reported WY South Dakota: no data reported SD Iowa: no data reported IA Illinois: no data reported IL Indiana: 952 units · 13.9 per 100k residents IN Ohio: 3,724 units · 31.6 per 100k residents OH Pennsylvania: 4,144 units · 32.0 per 100k residents PA New Jersey: 7,872 units · 84.7 per 100k residents NJ Massachusetts: 5,096 units · 72.8 per 100k residents MA California: 2,133 units · 5.5 per 100k residents CA Utah: no data reported UT Colorado: no data reported CO Nebraska: no data reported NE Missouri: 1,708 units · 27.6 per 100k residents MO Kentucky: 2,130 units · 47.1 per 100k residents KY West Virginia: 924 units · 52.2 per 100k residents WV Virginia: 3,416 units · 39.2 per 100k residents VA Maryland: 2,688 units · 43.5 per 100k residents MD Connecticut: 5,992 units · 166 per 100k residents CT Rhode Island: no data reported RI Arizona: no data reported AZ New Mexico: no data reported NM Kansas: no data reported KS Arkansas: no data reported AR Tennessee: 1,288 units · 18.1 per 100k residents TN North Carolina: no data reported NC South Carolina: no data reported SC Delaware: no data reported DE Oklahoma: 1,848 units · 45.6 per 100k residents OK Louisiana: 1,344 units · 29.4 per 100k residents LA Mississippi: no data reported MS Alabama: no data reported AL Georgia: 420 units · 3.8 per 100k residents GA D.C.: no data reported DC Hawaii: no data reported HI Texas: 7,252 units · 23.8 per 100k residents TX Florida: no data reported FL
Units reimbursed · per 100k residents
3.8166
gray = no data reported ⓘ
Colors are per 100,000 residents, so big states don’t automatically dominate. Tap or hover a state for its actual totals.
Tap or hover a state
…for its Medicaid breakdown
🏆 Top states by units · per 100k residents
1 Connecticut 166 /100k
2 New York 96.2 /100k
3 New Jersey 84.7 /100k
4 Massachusetts 72.8 /100k
5 West Virginia 52.2 /100k
6 Kentucky 47.1 /100k
7 Oklahoma 45.6 /100k
8 Maryland 43.5 /100k
National units — by quarter
💵 About the dollar figures: “reimbursed” is what Medicaid paid pharmacies before confidential manufacturer rebates, so the program’s real net cost is lower than these numbers. Fee-for-service and managed-care claims are combined unless split above. Source: CMS State Drug Utilization Data; per-100k rates use 2023 Census population estimates.

Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Camila — the program that covers self-administered drugs. 2 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Camila. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$1.9K
Claims incl. refills
108
Beneficiaries
61
Spend / beneficiary
$30.46
Spend / claim
$17.20
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.