Medroxyprogesterone
Medroxyprogesterone is a progestin hormone used in injections to prevent pregnancy (and, for one product, to manage endometriosis-associated pain) and in tablets to treat missed periods, abnormal uterine bleeding and protect the uterine lining in women taking estrogen after menopause.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 24 clinical label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
Medroxyprogesterone is a progestin (a form of progesterone), around since about 1959 and available as a generic, best known as the Depo-Provera birth control shot (it blocks ovulation and thickens cervical mucus; one version also eases endometriosis pain), with tablets for missed periods, abnormal uterine bleeding and protecting the uterine lining during estrogen therapy. It is usually well tolerated, though the shot often brings irregular spotting at first and some weight gain. The shot can thin bones, especially in teens, so use past 2 years is discouraged unless other options fall short, and with estrogen, the tablets carry a boxed warning for blood clots, stroke, heart attack, breast cancer and probable dementia.
Clinical pearls
- Fertility can be slow to return after the last shot, so plan to stop well before you hope to conceive.
- Carbamazepine, phenytoin, rifampin, St. John’s wort and other enzyme-inducing drugs can make it less effective as birth control.
- Smoking, heavy drinking, anorexia, or long-term steroids or seizure medicines add to the shot’s bone loss, so mention them first.
- It can alter some lab results, so tell any lab or pathologist reviewing a sample that you use it.
⚠️ FDA Boxed Warning — the FDA’s strongest safety alert ▾
The boxed warning is about estrogen plus progestin therapy, including medroxyprogesterone combined with estrogen after menopause. Do not use estrogen with a progestin to prevent heart disease, heart attack, stroke or dementia.
In large studies of postmenopausal women, this combination raised the risk of blood clots in the legs and lungs, stroke, heart attack and invasive breast cancer. Women aged 65 or older had a higher risk of probable dementia (decline in brain function). It is unknown whether this applies to younger postmenopausal women.
These therapies should be used at the lowest effective dose for the shortest time that meets treatment goals. Talk regularly with your healthcare provider about whether you still need treatment.
Patient information guide A plain-language walkthrough of Medroxyprogesterone, written from its FDA label.
What Medroxyprogesterone is used for
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Medroxyprogesterone is used differently depending on the product.
- Depo-Provera CI and medroxyprogesterone acetate injectable suspension (intramuscular): prevent pregnancy.
- Depo-SubQ Provera 104 (subcutaneous): prevents pregnancy and manages endometriosis-associated pain.
- Provera and medroxyprogesterone acetate tablets (oral): treat secondary amenorrhea (missed periods).
- Provera and medroxyprogesterone acetate tablets: treat abnormal uterine bleeding due to hormonal imbalance, without an underlying cause like fibroids or uterine cancer.
- Provera and medroxyprogesterone acetate tablets: help prevent endometrial hyperplasia in postmenopausal women with a uterus who take daily oral conjugated estrogens.
How Medroxyprogesterone works
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Depo-SubQ Provera 104 reduces gonadotropins, the hormones that signal the ovaries. This mainly prevents eggs from maturing and being released (ovulation). It also thickens cervical mucus, which adds to the birth control effect.
Lower estradiol levels are likely responsible for easing endometriosis-associated pain.
Medroxyprogesterone dosage
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How it is taken depends on the product. Always follow your prescriber and the label.
- Depo-Provera CI and medroxyprogesterone acetate injectable suspension: a deep muscle injection about every 3 months (13 weeks). The vial or syringe is shaken well first and sites are rotated.
- Depo-SubQ Provera 104: an injection under the skin about every 12 to 14 weeks, given only by a healthcare professional.
- Provera and medroxyprogesterone tablets: taken by mouth daily for a set number of days, timed to the condition being treated.
Dosing details from the FDA-approved label
From the Medroxyprogesterone prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
- Contraception (Depo-SubQ Provera 104, subcutaneous)
- 104 mg given subcutaneously into the anterior thigh or abdomen every 12 to 14 weeks
- Dosage does not need to be adjusted for body weight; use for longer than 2 years is not recommended unless other methods are considered inadequate
- Secondary amenorrhea (oral tablets)
- 5 or 10 mg daily for 5 to 10 days
- To induce optimum secretory transformation of an adequately estrogen-primed endometrium, 10 mg daily for 10 days
- Therapy may be started at any time
- Abnormal uterine bleeding due to hormonal imbalance in the absence of organic pathology (oral tablets)
- Beginning on the calculated 16th or 21st day of the menstrual cycle, 5 or 10 mg daily for 5 to 10 days
- 10 mg daily for 10 days beginning on the 16th day of the cycle is suggested for optimum secretory transformation
- Reduction of endometrial hyperplasia in postmenopausal women receiving daily 0.625 mg conjugated estrogens (oral tablets)
- 5 or 10 mg daily for 12 to 14 consecutive days per month, beginning on the 1st day or the 16th day of the cycle
- Start at the lowest dose; the lowest effective dose has not been determined
- Prevention of pregnancy (medroxyprogesterone acetate injectable suspension, intramuscular)
- 150 mg every 3 months (13 weeks) by deep intramuscular injection in the gluteal or deltoid muscle
Read the label’s full dosing text
DOSAGE AND ADMINISTRATION Secondary Amenorrhea Medroxyprogesterone acetate tablets may be given in dosages of 5 or 10 mg daily for 5 to 10 days. A dose for inducing an optimum secretory transformation of an endometrium that has been adequately primed with either endogenous or exogenous estrogen is 10 mg of medroxyprogesterone acetate daily for 10 days. In cases of secondary amenorrhea, therapy may be started at any time. Progestin withdrawal bleeding usually occurs within three to seven days after discontinuing medroxyprogesterone acetate therapy. Abnormal Uterine Bleeding Due to Hormonal Imbalance in the Absence of Organic Pathology Beginning on the calculated 16th or 21st day of the menstrual cycle, 5 or 10 mg of medroxyprogesterone acetate may be given daily for 5 to 10 days. To produce an optimum secretory transformation of an endometrium that has been adequately primed with either endogenous or exogenous estrogen, 10 mg of medroxyprogesterone acetate daily for 10 days beginning on the 16th day of the cycle is suggested. Progestin withdrawal bleeding usually occurs within three to seven days after discontinuing therapy with medroxyprogesterone acetate. Patients with a past history of recurrent episodes of abnormal uterine bleeding may benefit from planned menstrual cycling with medroxyprogesterone acetate. Reduction of Endometrial Hyperplasia in Postmenopausal Women Receiving Daily 0.625 mg Conjugated Estrogens When estrogen is prescribed for a postmenopausal woman with a uterus, a progestin should also be initiated to reduce the risk of endometrial cancer. A woman without a uterus does not need progestin. Use of estrogen, alone or in combination with a progestin, should be with the lowest effective dose and for the shortest duration consistent with treatment goals and risks for the individual woman. Patients should be re-evaluated periodically as clinically appropriate (for example, 3 to 6 month intervals) to determine if treatment is still necessary (see Error! Hyperlink reference not valid. ). For women who have a uterus, adequate diagnostic measures, such as endometrial sampling, when indicated, should be undertaken to rule out malignancy in cases of undiagnosed persistent or recurring abnormal vaginal bleeding.
Excerpted — the section continues on the label. Read the full Dosage and Administration section on DailyMed →
Medroxyprogesterone side effects
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The most common side effects reported with the injections include:
Common side effects
- Irregular, heavy, light or spotting bleeding
- Missed periods (amenorrhea)
- Headache
- Weight gain
- Injection site reactions (pain, lumps, dimpling)
- Vaginal infections such as yeast
- Abdominal pain
- Depression or mood changes
- Vaginal infections, belly pain, acne, nausea and mood changes
When to get medical help
- Call your doctor right away for signs of a blood clot or stroke, such as leg swelling or pain, chest pain, shortness of breath or sudden weakness.
- Get help right away for sudden loss of vision, bulging eyes, double vision or sudden migraine.
- Seek emergency care for signs of a severe allergic reaction (anaphylaxis).
- Call your doctor for yellowing of the skin or eyes (jaundice) or other signs of liver problems.
- Tell your doctor about severe belly pain, especially if you become pregnant, since it could be an ectopic pregnancy (pregnancy outside the uterus).
- Tell your doctor if depression returns or gets worse.
- Report bleeding that is heavy or does not stop.
- Report lumps in the breast or any breast changes.
Medroxyprogesterone warnings and precautions
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- Bone loss: the injections can significantly reduce bone mineral density, and recovery may be incomplete. Use beyond 2 years is not recommended unless other options are inadequate.
- Blood clots: stop treatment if a clot develops, unless there are no other acceptable birth control options.
- Breast cancer: women with a strong family history need careful monitoring, and those with a history of breast cancer should not use hormonal birth control.
- Other: liver problems, depression, fluid retention, weight gain, lowered glucose tolerance and bleeding changes.
- Fertility: return of ovulation can be delayed after stopping the injections.
- STDs: the injections do not protect against HIV or other sexually transmitted diseases.
Medroxyprogesterone interactions
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Some drugs and herbs can reduce how well hormonal birth control works.
- Enzyme inducers such as carbamazepine, phenytoin, rifampin, St. John’s wort, topiramate, barbiturates, bosentan, felbamate, griseofulvin and oxcarbazepine can lower hormone levels, so a back-up method may be needed.
- HIV protease inhibitors and non-nucleoside reverse transcriptase inhibitors can change progestin levels.
- Antibiotics: pregnancies have been reported, but studies show no consistent effect on hormone levels.
- Lab tests, including coagulation, lipids and glucose tolerance, may be affected.
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Medroxyprogesterone
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- Do not use the injections if you are or might be pregnant.
- Do not use them with a history of blood clots or cerebral vascular disease, breast cancer, significant liver disease or undiagnosed vaginal bleeding.
- Tell your prescriber about allergies, depression, diabetes, epilepsy, migraine, asthma, and heart or kidney problems.
- Tell your prescriber about osteoporosis risk factors, such as smoking, heavy alcohol use or long-term steroid use.
- Breastfeeding: small amounts pass into milk, with no adverse effects noted in infants. For exclusively breastfeeding mothers, the injection is started at or after 6 weeks postpartum.
- The injections are not indicated before a first period or after menopause.
Medroxyprogesterone overdose
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With estrogen plus progestin therapy, too much may cause nausea, vomiting, breast tenderness, dizziness, abdominal pain, drowsiness or fatigue, and withdrawal bleeding. Treatment is stopping the medicines and providing supportive care for symptoms.
What Medroxyprogesterone does in the body
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Progestins like Depo-SubQ Provera 104 lower gonadotropin levels, sex hormone binding globulin, and levels of steroids such as estradiol, progesterone and testosterone. Effects on cholesterol are inconsistent. Some lab values, such as clotting factors and liver tests, may rise.
How your body processes Medroxyprogesterone
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After a Depo-SubQ Provera 104 injection under the skin, drug levels rise within 24 hours and peak about a week later. About 86% of it binds to albumin in the blood. The liver breaks it down extensively, and most metabolites leave in the urine. Its half-life is about 40 days, which supports dosing every 12 to 14 weeks.
How to store Medroxyprogesterone
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Store at controlled room temperature 20° to 25°C (68° to 77°F) . Keep out of reach of children"
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Supplements & herbs that interact with Medroxyprogesterone
139 supplements and herbal products have documented interactions with Medroxyprogesterone in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 3
- Moderate · 95
- Minor · 41
Educational information from a licensed clinical database (Natural Medicines) — see our data sources & update cadence. Not medical advice: an interaction being documented does not mean it will happen to you; do not start or stop medications or supplements without professional guidance.
Medroxyprogesterone: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Medroxyprogesterone — the kind of thing our pharmacy team would talk through with you at the counter.
What is medroxyprogesterone used for?
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How often do I get the shot?
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What side effects should I expect?
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Does the shot affect my bones?
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Can other medicines affect how well it works?
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Will I be able to get pregnant after stopping?
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Is Medroxyprogesterone available over the counter?
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When was Medroxyprogesterone first available?
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Who makes Medroxyprogesterone?
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Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Medroxyprogesterone on HelloPharmacist
Medroxyprogesterone forms and strengths (how it comes)
Medroxyprogesterone is available in 2 forms. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Tablet
How this form is used
- Provera tablets treat secondary amenorrhea and abnormal uterine bleeding due to hormonal imbalance when no organic cause such as fibroids or uterine cancer is present.
- Provera tablets help prevent endometrial hyperplasia in postmenopausal women with a uterus who take daily oral conjugated estrogens.
- Provera tablets are taken by mouth once daily for a set number of days, depending on the condition.
- Provera tablets for secondary amenorrhea may be started at any time.
- Provera tablets for abnormal uterine bleeding are started on a set day of the menstrual cycle.
Injection
How this form is used
- Depo-Provera CI is used to prevent pregnancy in females of reproductive potential.
- Depo-SubQ Provera 104 is used to prevent pregnancy and manage endometriosis-associated pain in females of reproductive age.
- Medroxyprogesterone acetate injectable suspension is used to prevent pregnancy in females of reproductive potential.
- Depo-Provera CI is given by deep intramuscular injection into the buttock or upper arm about every 3 months (13 weeks).
- Depo-SubQ Provera 104 is given only by a healthcare professional, under the skin of the thigh or abdomen, about every 12 to 14 weeks.
- Depo-Provera CI is not recommended for more than 2 years unless other birth control options are considered inadequate.
- Depo-SubQ Provera 104 is not recommended for more than 2 years unless other options are considered inadequate.
Medroxyprogesterone on the U.S. market: products, makers and brands
How Medroxyprogesterone appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
23 companies list 48 Medroxyprogesterone product records with the FDA, mostly as tablet, injection; the earliest marketing or approval year on record is 1959. Brand names on the directory include Provera, Amen, Curretab and 4 more; the rest are generics.
FDA-listed product records by dose form (tablet variants merged) — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
Also listed with the FDA, not a patient dose form: Powder (15) — bulk drug substance sold to compounders/manufacturers and multi-item kits. These aren’t counted in the dose-form total above.
Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
How widely Medroxyprogesterone is used (Medicaid data)
A general measure of how commonly Medroxyprogesterone is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Medroxyprogesterone is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Medroxyprogesterone prescribed? Of the 1,601 medications we measure, Medroxyprogesterone ranks #153 by Medicaid prescriptions — more than 90% of them.
Utilization by Medroxyprogesterone product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
1 ML medroxyprogesterone acetate 150 MG/ML Injection Most dispensed
Summed across the 21 of 37 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1000126
1 ML medroxyprogesterone acetate 150 MG/ML Prefilled Syringe
Summed across the 6 of 12 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1000153
medroxyprogesterone acetate 10 MG Oral Tablet
Summed across the 5 of 49 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1000114
medroxyprogesterone acetate 5 MG Oral Tablet
Summed across the 3 of 13 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1000141
medroxyprogesterone acetate 2.5 MG Oral Tablet
Summed across the 3 of 22 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1000135
0.65 ML medroxyprogesterone acetate 160 MG/ML Prefilled Syringe
Summed across the 1 of 1 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1000156
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Medroxyprogesterone, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 39 of 134 listed Medroxyprogesterone NDCs with Medicaid activity.
Compare Medroxyprogesterone products
A representative set of FDA-listed product records for Medroxyprogesterone — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Injection | ||||
| 150 mg/mL | Intramuscular | A-S Medication Solutions × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 150 mg/mL | Intramuscular | Amneal Pharmaceuticals LLC × 2 listings | ANDA | View NDC → |
| 150 mg/mL | Intramuscular | Amneal Pharmaceuticals NY LLC | ANDA | View NDC → |
| 150 mg/mL | Intramuscular | Amphastar Pharmaceuticals, Inc. × 2 listings | ANDA | View NDC → |
| 150 mg/mL | Intramuscular | Eugia US LLC × 2 listings | ANDA | View NDC → |
| 150 mg/mL | Intramuscular | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 150 mg/mL | Intramuscular | Mylan Institutional LLC | ANDA | View NDC → |
| 104 mg/0.65 mL | Subcutaneous | Pharmacia & Upjohn Company LLC | NDA | View NDC → |
| 150 mg/mL | Intramuscular | Pharmacia & Upjohn Company LLC × 2 listings | NDA | View NDC → |
| 150 mg/mL | Intramuscular | Prasco Laboratories × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 150 mg/mL | Intramuscular | Remedyrepack Inc. | ANDA | View NDC → |
| 150 mg/mL | Intramuscular | Sun Pharmaceutical Industries, Inc. × 2 listings | ANDA | View NDC → |
| 150 mg/mL | Intramuscular | Xiromed LLC | ANDA | View NDC → |
| 💊Tablet | ||||
| 2.5 mg | Oral | A-S Medication Solutions | ANDA | View NDC → |
| 5 mg | Oral | A-S Medication Solutions | ANDA | View NDC → |
| 10 mg | Oral | A-S Medication Solutions | ANDA | View NDC → |
| 10 mg | Oral | American Health Packaging | ANDA | View NDC → |
| 2.5 mg | Oral | Bryant Ranch Prepack | ANDA | View NDC → |
| 5 mg | Oral | Bryant Ranch Prepack | ANDA | View NDC → |
| 10 mg | Oral | Bryant Ranch Prepack × 2 listings | ANDA | View NDC → |
| 2.5 mg | Oral | Coupler LLC | ANDA | View NDC → |
| 2.5 mg | Oral | Mylan Pharmaceuticals Inc. | NDA AUTHORIZED GENERIC | View NDC → |
| 5 mg | Oral | Mylan Pharmaceuticals Inc. | NDA AUTHORIZED GENERIC | View NDC → |
| 10 mg | Oral | Mylan Pharmaceuticals Inc. | NDA AUTHORIZED GENERIC | View NDC → |
| 10 mg | Oral | Northwind Health Company, LLC | ANDA | View NDC → |
| 10 mg | Oral | NuCare Pharmaceuticals,Inc. | ANDA | View NDC → |
| 2.5 mg | Oral | PD-Rx Pharmaceuticals, Inc. | ANDA | View NDC → |
| 10 mg | Oral | PD-Rx Pharmaceuticals, Inc. | ANDA | View NDC → |
| 2.5 mg | Oral | Pharmacia & Upjohn Company LLC | NDA | View NDC → |
| 5 mg | Oral | Pharmacia & Upjohn Company LLC | NDA | View NDC → |
| 10 mg | Oral | Pharmacia & Upjohn Company LLC | NDA | View NDC → |
| 10 mg | Oral | PharmPak, Inc. | ANDA | View NDC → |
| 10 mg | Oral | Preferred Pharmaceuticals, Inc. | ANDA | View NDC → |
| 5 mg | Oral | Preferred Pharmaceuticals Inc. | ANDA | View NDC → |
| 10 mg | Oral | Proficient Rx LP | ANDA | View NDC → |
| 2.5 mg | Oral | Remedyrepack Inc. | ANDA | View NDC → |
| 10 mg | Oral | Remedyrepack Inc. | ANDA | View NDC → |
| 2.5 mg | Oral | Teva Pharmaceuticals USA, Inc. | ANDA | View NDC → |
| 5 mg | Oral | Teva Pharmaceuticals USA, Inc. | ANDA | View NDC → |
| 10 mg | Oral | Teva Pharmaceuticals USA, Inc. | ANDA | View NDC → |
Showing 48 of 48 products — FDA National Drug Code Directory. See every product, package size and price: browse all 48 Medroxyprogesterone NDCs →
Medroxyprogesterone side effects reported to the FDA (FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Medroxyprogesterone — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Medroxyprogesterone in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
Medroxyprogesterone FDA approval history
How Medroxyprogesterone went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Medroxyprogesterone recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
The FDA’s enforcement reports list 2 Medroxyprogesterone recalls since July 2021. One of them is still ongoing and is listed first. A recall names specific lots from one company, so check the lot number on your own bottle rather than assuming every product is affected; your pharmacist can check whether your supply came from an affected lot.
- medroxyPROGESTERone Acetate Injectable Suspension, USP, 150mg per mL, Rx only, 1 mL Single-Dose Vial, Mfd in India for: Eugia US LLC, NJ 08520 NDC 55150-329-01 Shipper label: medroxyPROGESTERone Acet… Lots: Lot No.: 1MP24069, Exp.: 08/2026 FDA record D-0185-2025 →
- medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured by Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, I… Lots: Lot #: HAC1951A, Exp 06/2023 FDA record D-1145-2022 →
Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.
RxCUI 6691 4 dose forms · 13 strengths
-
Dose form (SCDF) Injectable Suspension RxCUI 378653In current FDA listingsClinical drug / strength (SCD) acetate 160 MG/MLRxCUI 1000374acetate 200 MG/MLRxCUI 1000378 -
Dose form (SCDF) Injection RxCUI 1738611In current FDA listingsClinical drug / strength (SCD) 1 ML medroxyprogesterone acetate 150 MG/MLRxCUI 1000126 -
Dose form (SCDF) Oral Tablet RxCUI 372739In current FDA listingsClinical drug / strength (SCD) acetate 10 MGRxCUI 1000114acetate 100 MGRxCUI 1000364acetate 2.5 MGRxCUI 1000135acetate 200 MGRxCUI 1000376acetate 250 MGRxCUI 1000380acetate 400 MGRxCUI 1000384acetate 5 MGRxCUI 1000141acetate 500 MGRxCUI 1000386 -
Dose form (SCDF) Prefilled Syringe RxCUI 727610No current FDA listingClinical drug / strength (SCD) 0.65 ML medroxyprogesterone acetate 160 MG/MLRxCUI 10001561 ML medroxyprogesterone acetate 150 MG/MLRxCUI 1000153
Look up RxCUI 6691 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
Medroxyprogesterone supply and shortage status
Whether Medroxyprogesterone is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
💵 What Medroxyprogesterone costs pharmacies (NADAC benchmark)
The national average invoice price pharmacies pay for the drug itself, from CMS's NADAC survey (data as of Sep 30, 2026). This is a supply-cost benchmark — not a retail price and not what you'd pay at the counter.
| Form | Strength | Pharmacy acquisition benchmark | |
|---|---|---|---|
| Injection, Suspension · Intramuscular | 150 mg/mL | $50.99 per mL | NDC details & price history |
| Injection, Suspension, Extended Release · Intramuscular | 150 mg/mL | $18.85–$22.85 per mL | NDC details & price history |
| Injection, Suspension · Subcutaneous | 104 mg/0.65 mL | $77.43 per mL | NDC details & price history |
Source: CMS National Average Drug Acquisition Cost (NADAC), a survey of retail pharmacy invoice prices. Benchmarks shown are the range across package sizes of a representative product for each form and strength — other manufacturers' products may differ.
Medroxyprogesterone brand names
Medroxyprogesterone is sold under 7 brand names in the FDA directory — Provera, Amen, Curretab, Cycrin and others. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Medroxyprogesterone: manufacturers and labelers
23 companies list Medroxyprogesterone products with the FDA. By number of product records, the largest are Pharmacia & Upjohn Company LLC, A-S Medication Solutions, Bryant Ranch Prepack. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
Medroxyprogesterone drug class (RxNorm)
Medroxyprogesterone belongs to the Progestin class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
Sources for this Medroxyprogesterone page
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. PharmPak, Inc. is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →