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Cefadroxil 500 mg Capsule, 50-count — NDC 16714-388-01 (Billing 16714-0388-01)

by NorthStar Rx LLC · 50 CAPSULE in 1 BOTTLE

This is a package of 50 capsules of Cefadroxil 500 mg Capsule from NorthStar Rx LLC, marketed since Jan 2007 and currently FDA-listed; retail pharmacies pay about $0.2690 per capsule (NADAC).

NDC 16714-0388-01
🏷️ FDA NDC (as labeled) 16714-388-01 billing pads the product segment with a zero
This package
Contains50-count Cost per ea$0.2690 NADAC Per package$13.45 / 50 capsules Pack sizes2 compare ↓
Also priced by: Medicaid pays $1.30/unit · Part D plans $0.4938/unit — full pricing hub ↓
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) 16714-388-01
Product NDC 16714-388
11-digit billing NDC 16714038801
NCPDP billing unit EA — each (per item)
RxCUI 309049
UNII 280111G160
Application # ANDA065352
SPL Set ID 17123057-58c7-401a-b87d-8c4c0764bbf6
Established class (EPC) Cephalosporin Antibacterial
Chemical class Cephalosporins
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2007-01-25
Route ORAL
Dosage form CAPSULE
Substance CEFADROXIL
TE code (Orange Book) AB · RLD · RS

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

GPI-14 02100010000105
GPI class Cefadroxil
GCN Seq No 048262
GCN 45341
HICL code 022796
Ingredient (HICL) Cefadroxil
HIC1 code W
Therapeutic class — broad (HIC1) Anti-Infecting Agents
HIC2 code W1
Therapeutic class — intermediate (HIC2) Antibiotics
HIC3 code W1W
Therapeutic class — specific (HIC3) Cephalosporin Antibiotics - 1St Generation
AHFS code 08:12.06.04
AHFS class 1St Generation Cephalosporin Antibiotics
FDB label name CEFADROXIL 500 MG CAPSULE
FDB brand name Cefadroxil
Legend status F — Federal legend — prescription drug or device
Quick answers
  • GSN (GCN sequence number): 048262
  • GCN: 45341
  • GPI-14 (Medi-Span): 02100010000105
  • HICL (First Databank): 022796
  • AHFS class code: 08:12.06.04
  • RxCUI (RxNorm): 309049
Why two NDCs? The FDA registers this code as 16714-388-01 — 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 → 16714-0388-01. 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 Cephalosporin Antibacterial class.

Pharmacologic class Cephalosporin Antibacterial
Drug family (ATC) First-generation cephalosporins
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 CEFADROXIL 500 MG CAPSULE Ingredient Cefadroxil
📗 Our plain-language guide HelloPharmacist
  • It is an antibiotic for bacterial infections of the urinary tract, the skin, and the throat or tonsils (strep). It will not help colds, flu or other viral illnesses. Your prescribe...
  • You can take it with or without food. If it upsets your stomach, taking it with a meal may help. Follow the directions on your pharmacy label for how often to take it.
  • Take it for the full course your prescriber gave you. For strep throat or tonsillitis, treatment is at least 10 days. Stopping early can let the infection come back.
  • Tell your prescriber first. Some people with a penicillin allergy also react to cephalosporins like cefadroxil, up to about 10% in those with a history of penicillin allergy. If yo...
📖 Read our full Cefadroxil guide →
7
Nutrient depletion considerations

Cefadroxil may be associated with lower levels of 7 nutrients — worth a chat with your pharmacist, not a cause for alarm.

An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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 $0.269 $13.45 / 50 capsules
Medicaid paysCMS SDUD · 12 mo $1.30 $65.16 / 50 capsules
Medicare drug plans payPart D · Q2 2026 $0.4938 $24.69 / 50 capsules
NADAC price history (per ea) — tap or hover for the price & month
Jan 2022 Aug 2022 Jan 2026 Sep 2026 $0.312 $0.193
▲ Up 39% over the last 24 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 Per unit Per pack Marketing startMarketing endStatus
16714-0388-01 You're viewing this 50 CAPSULE in 1 BOTTLE $0.2690 / ea $13.45 2007-01-25 — Active
16714-0388-02 16714-388-02 Main listing 100 CAPSULE in 1 BOTTLE $0.2690 / ea $26.90 2007-01-25 — Active

You're viewing the smallest of 2 pack sizes for this product.

This pack has the lowest per-ea cost of the 2 priced pack sizes ($0.2690 NADAC).

This pack accounts for about 46% of this product's recent Medicaid fills; most go to the 100 capsules pack. See all packs ↓

Pack size FAQ

What quantity is in this package?
This is a 50-count package — 50 capsule in 1 bottle.
How does this package differ from NDC 16714-0388-02?
Both are Cefadroxil 500 mg Capsule — the drug itself is identical. This page's package is the 50-count one, while NDC 16714-0388-02 is the 100 capsules package.
What NDC number is used to bill for this package of Cefadroxil 500 mg Capsule?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Prices are the latest CMS NADAC pharmacy acquisition cost per NDC; per-pack figures are per-unit × pack quantity, shown only when the pack is denominated in the same measure NADAC prices.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Cefadroxil 500 mg 00093-3196-01 Teva 100 capsules $0.269 AB Availability likely —
Cefadroxil 500 mgthis 16714-0388-01 NorthStar 50 capsules $0.269 AB Availability likely —
Cefadroxil 500 mg 57237-0096-01 Rising 100 capsules $0.269 AB Availability likely —
Cefadroxil 500 mg 65862-0085-01 Aurobindo 100 capsules $0.269 AB Availability likely —
Cefadroxil 500 mg 68180-0180-01 Lupin 100 capsules $0.269 AB Availability likely —
Cefadroxil 500 mg 43063-0553-10 PD-Rx 10 capsules — AB FDA listed —
Cefadroxil 500 mg 43063-0595-20 PD-Rx 20 capsules — AB FDA listed —
Cefadroxil 500 mg 50090-6050-00 A-S 10 capsules — AB FDA listed —
Cefadroxil 500 mg 63187-0883-06 Proficient 6 capsules — AB FDA listed —
Cefadroxil 500 mg 63629-7987-01 Bryant 20 capsules — AB FDA listed —
Cefadroxil 500 mg 63629-7988-01 Bryant 30 capsules — AB FDA listed —
Cefadroxil 500 mg 63629-8253-01 Bryant 14 capsules — AB FDA listed —
Cefadroxil 500 mg 63629-9456-01 Bryant 20 capsules — AB FDA listed —
Cefadroxil 500 mg 67296-0491-01 Redpharm 20 capsules — AB FDA listed —
Cefadroxil 500 mg 67296-1727-01 RedPharm 14 capsules — AB FDA listed —
Cefadroxil 500 mg 67296-2199-01 Redpharm 14 capsules — AB FDA listed —
Cefadroxil 500 mg 67296-2221-02 Redpharm 20 capsules — AB FDA listed —
Cefadroxil 500 mg 68071-3597-06 NuCare 6 capsules — AB FDA listed —
Cefadroxil 500 mg 68071-4515-01 NuCare 10 capsules — AB FDA listed —
Cefadroxil 500 mg 68071-4690-06 NuCare 6 capsules — AB FDA listed —
Cefadroxil 500 mg 68071-4938-01 NuCare 10 capsules — AB FDA listed —
Cefadroxil 500 mg 68071-5234-06 NuCare 6 capsules — AB FDA listed —
Cefadroxil 500 mg 68788-8261-02 Preferred 50 capsules — AB FDA listed —
Cefadroxil 500 mg 68788-8479-02 Preferred 20 capsules — AB FDA listed —
Cefadroxil 500 mg 70518-3580-00 REMEDYREPACK 20 capsules — AB FDA listed —
Cefadroxil 500 mg 72189-0103-06 DIRECT 6 capsules — AB FDA listed —
Cefadroxil 500 mg 72189-0445-06 Direct_Rx 6 capsules — AB FDA listed —
Cefadroxil 500 mg 72189-0506-20 Direct_Rx 20 capsules — AB FDA listed —
Cefadroxil 500 mg 80425-0198-01 Advanced 10 capsules — AB FDA listed —
Cefadroxil 500 mg 80425-0400-01 Advanced 10 capsules — AB FDA listed —
Cefadroxil 500 mg 80425-0432-01 Advanced 10 capsules — AB 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

🏛️
2007
On the market since
Jan 2007
📍
2026
Currently FDA-listed
19 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

LabelerNorthStar Rx LLC
Application holderAUROBINDO PHARMA LTD
FDA applicationANDA065352 (ANDA)
Labeler code16714
First marketedJan 2007
Product typeHuman Prescription Drug
Portfolio414 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 204 words ▾

INDICATIONS AND USAGE Cefadroxil is indicated for the treatment of patients with infection caused by susceptible strains of the designated organisms in the following diseases: Urinary tract infections caused by E. coli, P. mirabilis, and Klebsiella species. Skin and skin structure infections caused by staphylococci and/or streptococci. Pharyngitis and/or tonsillitis caused by Streptococcus pyogenes (Group A beta-hemolytic streptococci).

Note: Only penicillin by the intramuscular route of administration has been shown to be effective in the prophylaxis of rheumatic fever. Cefadroxil is generally effective in the eradication of streptococci from the oropharynx. However, data establishing the efficacy of cefadroxil for the prophylaxis of subsequent rheumatic fever are not available.

Note: Culture and susceptibility tests should be initiated prior to and during therapy. Renal function studies should be performed when indicated. To reduce the development of drug-resistant bacteria and maintain the effectiveness of cefadroxil and other antibacterial drugs, cefadroxil should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria.

When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemology and susceptibility patterns may contribute to the empiric selection of therapy.

⏱️ Dosage and Administration ~1 min read ▾

DOSAGE AND ADMINISTRATION Cefadroxil is acid-stable and may be administered orally without regard to meals. Administration with food may be helpful in diminishing potential gastrointestinal complaints occasionally associated with oral cephalosporin therapy. Adults Urinary Tract Infections: For uncomplicated lower urinary tract infections (i.e., cystitis) the usual dosage is 1 or 2 g per day in a single (q.d.) or divided doses (b.i.d.).

For all other urinary tract infections the usual dosage is 2 g per day in divided doses (b.i.d.). Skin and Skin Structure Infections: For skin and skin structure infections the usual dosage is 1 g per day in single (q.d.) or divided doses (b.i.d.). Pharyngitis and Tonsillitis: Treatment of group A beta-hemolytic streptococcal pharyngitis and tonsillitis—1 g per day in single (q.d.) or divided doses (b.i.d.) for 10 days.

Children For urinary tract infections, the recommended daily dosage for children is 30 mg/kg/day in divided doses every 12 hours. For pharyngitis, tonsillitis, and impetigo, the recommended daily dosage for children is 30 mg/kg/day in a single dose or in equally divided doses every 12 hours. For other skin and skin structure infections, the recommended daily dosage is 30 mg/kg/day in equally divided doses every 12 hours.

In the treatment of beta-hemolytic streptococcal infections, a therapeutic dosage of cefadroxil should be administered for at least 10 days. Renal Impairment In patients with renal impairment, the dosage of cefadroxil should be adjusted according to creatinine clearance rates to prevent drug accumulation. The following schedule is suggested.

In adults, the initial dose is 1000 mg of cefadroxil and the maintenance dose (based on the creatinine clearance rate [mL/min/1.73 m 2 ]) is 500 mg at the time intervals listed below. Creatinine Clearances Dosage Interval 0 to 10 mL/min 36 hours 10 to 25 mL/min 24 hours 25 to 50 mL/min 12 hours Patients with creatinine clearance rates over 50 mL/min may be treated as if they were patients having normal renal function.

⛔ Contraindications 15 words ▾

CONTRAINDICATIONS Cefadroxil is contraindicated in patients with known allergy to the cephalosporin group of antibiotics.

⚠️ Warnings ~1 min read ▾

WARNINGS BEFORE THERAPY WITH CEFADROXIL IS INSTITUTED, CAREFUL INQUIRY SHOULD BE MADE TO DETERMINE WHETHER THE PATIENT HAS HAD PREVIOUS HYPERSENSITIVITY REACTIONS TO CEFADROXIL, CEPHALOSPORINS, PENICILLINS, OR OTHER DRUGS. IF THIS PRODUCT IS TO BE GIVEN TO PENICILLIN-SENSITIVE PATIENTS, CAUTION SHOULD BE EXERCISED BECAUSE CROSS-SENSITIVITY AMONG BETA-LACTAM ANTIBIOTICS HAS BEEN CLEARLY DOCUMENTED AND MAY OCCUR IN UP TO 10% OF PATIENTS WITH A HISTORY OF PENICILLIN ALLERGY. IF AN ALLERGIC REACTION TO CEFADROXIL OCCURS, DISCONTINUE THE DRUG.

SERIOUS ACUTE HYPERSENSITIVITY REACTIONS MAY REQUIRE TREATMENT WITH EPINEPHRINE AND OTHER EMERGENCY MEASURES, INCLUDING OXYGEN, INTRAVENOUS FLUIDS, INTRAVENOUS ANTIHISTAMINES, CORTICOSTEROIDS, PRESSOR AMINES, AND AIRWAY MANAGEMENT, AS CLINICALLY INDICATED. Clostridium difficile associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including cefadroxil, and may range in severity from mild diarrhea to fatal colitis. Treatment with antibacterial agents alters the normal flora of the colon leading to overgrowth of C. difficile .

C. difficile produces toxins A and B which contribute to the development of CDAD. Hypertoxin producing strains of C. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhea following antibiotic use.

Careful medical history is necessary since CDAD has been reported to occur over two months after the administration of antibacterial agents. If CDAD is suspected or confirmed, ongoing antibiotic use not directed against C. difficile may need to be discontinued. Appropriate fluid and electrolyte management, protein supplementation, antibiotic treatment of C. difficile , and surgical evaluation should be instituted as clinically indicated.

🤒 Adverse Reactions 219 words ▾

ADVERSE REACTIONS Gastrointestinal Onset of pseudomembranous colitis symptoms may occur during or after antibiotic treatment (see WARNINGS ). Dyspepsia, nausea and vomiting have been reported rarely. Diarrhea has also occurred.

Hypersensitivity Allergies (in the form of rash, urticaria, angioedema, and pruritus) have been observed. These reactions usually subsided upon discontinuation of the drug. Anaphylaxis has also been reported.

Other Other reactions have included hepatic dysfunction including cholestasis and elevations in serum transaminase, genital pruritus, genital moniliasis, vaginitis, moderate transient neutropenia, fever. Agranulocytosis, thrombocytopenia, idiosyncratic hepatic failure, erythema multiforme, Stevens-Johnson syndrome, serum sickness, and arthralgia have been rarely reported. In addition to the adverse reactions listed above which have been observed in patients treated with cefadroxil, the following adverse reactions and altered laboratory tests have been reported for cephalosporin-class antibiotics: Toxic epidermal necrolysis, abdominal pain, superinfection, renal dysfunction, toxic nephropathy, aplastic anemia, hemolytic anemia, hemorrhage, prolonged prothrombin time, positive Coombs’ test, increased BUN, increased creatinine, elevated alkaline phosphatase, elevated aspartate aminotransferase (AST), elevated alanine aminotransferase (ALT), elevated bilirubin, elevated LDH, eosinophilia, pancytopenia, neutropenia.

Several cephalosporins have been implicated in triggering seizures, particularly in patients with renal impairment, when the dosage was not reduced (see DOSAGE AND ADMINISTRATION and OVERDOSAGE ). If seizures associated with drug therapy occur, the drug should be discontinued. Anticonvulsant therapy can be given if clinically indicated.

🔄 Drug / Laboratory Test Interactions 62 words ▾

Drug/Laboratory Test Interactions Positive direct Coombs’ tests have been reported during treatment with the cephalosporin antibiotics. In hematologic studies or in transfusion cross-matching procedures when antiglobulin tests are performed on the minor side or in Coombs’ testing of newborns whose mothers have received cephalosporin antibiotics before parturition, it should be recognized that a positive Coombs’ test may be due to the drug.

🤰 Pregnancy 73 words ▾

Pregnancy: Pregnancy Category B Reproduction studies have been performed in mice and rats at doses up to 11 times the human dose and have revealed no evidence of impaired fertility or harm to the fetus due to cefadroxil monohydrate. There are, however, no adequate and well controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

🧒 Pediatric Use 7 words ▾

Pediatric Use (See DOSAGE AND ADMINISTRATION .)

🧓 Geriatric Use 193 words ▾

Geriatric Use Of approximately 650 patients who received cefadroxil for the treatment of urinary tract infections in three clinical trials, 28% were 60 years and older, while 16% were 70 years and older. Of approximately 1000 patients who received cefadroxil for the treatment of skin and skin structure infection in 14 clinical trials, 12% were 60 years and older while 4% were 70 years and over. No overall differences in safety were observed between the elderly patients in these studies and younger patients.

Clinical studies of cefadroxil for the treatment of pharyngitis or tonsillitis did not include sufficient numbers of patients 65 years and older to determine whether they respond differently from younger patients. Other reported clinical experience with cefadroxil has not identified differences in responses between elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out. Cefadroxil is substantially excreted by the kidney, and dosage adjustment is indicated for patients with renal impairment (see DOSAGE AND ADMINISTRATION: Renal Impairment ).

Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.

🆘 Overdosage 76 words ▾

OVERDOSAGE A study of children under six years of age suggested that ingestion of less than 250 mg/kg of cephalosporins is not associated with significant outcomes. No action is required other than general support and observation. For amounts greater than 250 mg/kg, induce gastric emptying. In five anuric patients, it was demonstrated that an average of 63% of a 1 g oral dose is extracted from the body during a 6 to 8 hour hemodialysis session.

🧬 Clinical Pharmacology ~1 min read ▾

CLINICAL PHARMACOLOGY Cefadroxil is rapidly absorbed after oral administration. Following single doses of 500 mg and 1000 mg, average peak serum concentrations were approximately 16 and 28 mcg/mL, respectively. Measurable levels were present 12 hours after administration.

Over 90% of the drug is excreted unchanged in the urine within 24 hours. Peak urine concentrations are approximately 1800 mcg/mL during the period following a single 500 mg oral dose. Increases in dosage generally produce a proportionate increase in cefadroxil urinary concentration.

The urine antibiotic concentration, following a 1 g dose, was maintained well above the MIC of susceptible urinary pathogens for 20 to 22 hours. Microbiology In vitro tests demonstrate that the cephalosporins are bactericidal because of their inhibition of cell-wall synthesis. Cefadroxil has been shown to be active against the following organisms both in vitro and in clinical infections (see INDICATIONS AND USAGE ): Beta-hemolytic streptococci Staphylococci, including penicillinase-producing strains Streptococcus (Diplococcus) pneumoniae Escherichia coli Proteus mirabilis Klebsiella species Moraxella (Branhamella) catarrhalis Note: Most strains of Enterococcus faecalis (formerly Streptococcus faecalis ) and Enterococcus faecium (formerly Streptococcus faecium ) are resistant to cefadroxil.

It is not active against most strains of Enterobacter species, Morganella morganii (formerly Proteus morganii ), and P. vulgaris . It has no activity against Pseudomonas species and Acinetobacter calcoaceticus (formerly Mima and Herellea species). Susceptibility Testing For specific information regarding susceptibility test interpretive criteria and associated test methods and quality control standards recognized by FDA for this drug, please see: https://www.fda.gov/STIC.

📦 How Supplied / Storage and Handling 94 words ▾

HOW SUPPLIED Cefadroxil Capsules, USP 500 mg are maroon/white colored, size “0” hard gelatin capsules filled with white to off-white granular free flowing powder and imprinted with “C” on maroon opaque cap and “97” on white opaque body with black ink. Bottles of 50 NDC 16714-388-01 Bottles of 100 NDC 16714-388-02 Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Manufactured for: Northstar Rx LLC Memphis, TN 38141.

Manufactured by: Aurobindo Pharma Limited Chitkul (V)-502 307, India M.L.No.: 78/MD/AP/96/F/B/R Revised: 09/2018

📋 Description 104 words ▾

DESCRIPTION Cefadroxil, USP is a semisynthetic cephalosporin antibiotic intended for oral administration. It is a white to yellowish-white crystalline powder. It is soluble in water and it is acid-stable.

It is chemically designated as 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[amino(4-hydroxyphenyl)acetyl]amino]-3-methyl-8-oxo-, monohydrate, [6R-[6α,7β(R*)]]-. It has the formula C 16 H 17 N 3 O 5 S · H 2 O and the molecular weight of 381.40. It has the following structural formula: Cefadroxil capsules contain the following inactive ingredients: Lactose monohydrate, magnesium stearate, FD&C Blue No.1, D&C Red No.28, FD&C Red No.

40, titanium dioxide, gelatin, sodium lauryl sulphate, and edible black ink (black iron oxide). Chemical Structure

💬 Information for Patients 173 words ▾

Information for Patients Patients should be counseled that antibacterial drugs including cefadroxil should only be used to treat bacterial infections. They do not treat viral infections (e.g., the common cold). When cefadroxil is prescribed to treat a bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed.

Skipping doses or not completing the full course of therapy may (1) decrease the effectiveness of the immediate treatment and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by cefadroxil or other antibacterial drugs in the future. Diarrhea is a common problem caused by antibiotics which usually ends when the antibiotic is discontinued. Sometimes after starting treatment with antibiotics, patients can develop watery and bloody stools (with or without stomach cramps and fever) even as late as two or more months after having taken the last dose of the antibiotic.

If this occurs, patients should contact their physician as soon as possible.

⚠️ Precautions ~3 min read ▾

PRECAUTIONS General Cefadroxil should be used with caution in the presence of markedly impaired renal function (creatinine clearance rate of less than 50 mL/min/1.73 m 2 ). (See DOSAGE AND ADMINISTRATION .) In patients with known or suspected renal impairment, careful clinical observation and appropriate laboratory studies should be made prior to and during therapy. Prescribing cefadroxil in the absence of a proven or strongly suspected bacterial infection or a prophylactic indication is unlikely to provide benefit to the patient and increases the risk of the development of drug-resistant bacteria.

Prolonged use of cefadroxil may result in the overgrowth of nonsusceptible organisms. Careful observation of the patient is essential. If superinfection occurs during therapy, appropriate measures should be taken.

Cefadroxil should be prescribed with caution in individuals with history of gastrointestinal disease particularly colitis. Information for Patients Patients should be counseled that antibacterial drugs including cefadroxil should only be used to treat bacterial infections. They do not treat viral infections (e.g., the common cold).

When cefadroxil is prescribed to treat a bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. Skipping doses or not completing the full course of therapy may (1) decrease the effectiveness of the immediate treatment and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by cefadroxil or other antibacterial drugs in the future. Diarrhea is a common problem caused by antibiotics which usually ends when the antibiotic is discontinued.

Sometimes after starting treatment with antibiotics, patients can develop watery and bloody stools (with or without stomach cramps and fever) even as late as two or more months after having taken the last dose of the antibiotic. If this occurs, patients should contact their physician as soon as possible. Drug/Laboratory Test Interactions Positive direct Coombs’ tests have been reported during treatment with the cephalosporin antibiotics.

In hematologic studies or in transfusion cross-matching procedures when antiglobulin tests are performed on the minor side or in Coombs’ testing of newborns whose mothers have received cephalosporin antibiotics before parturition, it should be recognized that a positive Coombs’ test may be due to the drug. Carcinogenesis, Mutagenesis, Impairment of Fertility No long-term studies have been performed to determine carcinogenic potential. No genetic toxicity tests have been performed.

Pregnancy: Pregnancy Category B Reproduction studies have been performed in mice and rats at doses up to 11 times the human dose and have revealed no evidence of impaired fertility or harm to the fetus due to cefadroxil monohydrate. There are, however, no adequate and well controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

Labor and Delivery Cefadroxil has not been studied for use during labor and delivery. Treatment should only be given if clearly needed. Nursing Mothers Caution should be exercised when cefadroxil monohydrate is administered to a nursing mother.

Pediatric Use (See DOSAGE AND ADMINISTRATION .) Geriatric Use Of approximately 650 patients who received cefadroxil for the treatment of urinary tract infections in three clinical trials, 28% were 60 years and older, while 16% were 70 years and older. Of approximately 1000 patients who received cefadroxil for the treatment of skin and skin structure infection in 14 clinical trials, 12% were 60 years and older while 4% were 70 years and over. No overall differences in safety were observed between the elderly patients in these studies and younger patients.

Clinical studies of cefadroxil for the treatment of pharyn… [Excerpted — this section continues on DailyMed.]

🍼 Nursing Mothers 15 words ▾

Nursing Mothers Caution should be exercised when cefadroxil monohydrate is administered to a nursing mother.

📄 Carcinogenesis, Mutagenesis, Impairment of Fertility 22 words ▾

Carcinogenesis, Mutagenesis, Impairment of Fertility No long-term studies have been performed to determine carcinogenic potential. No genetic toxicity tests have been performed.

📄 Package Label / Principal Display Panel 34 words ▾

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 500 mg (50 Capsule Bottle) R x only NDC 16714-388-01 Cefadroxil Capsules, USP 500 mg 50 Capsules NorthStaRx TM PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 500 mg (50 Capsule Bottle)

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
5.8K
Units reimbursed last 4 qtrs
127.2K
Gross reimbursed last 4 qtrs
$165.8K
Avg / prescription
$28.44
Avg / unit
$1.3031
Latest quarter Q1 2026
1.1KRx
Medicaid pays / ea
$1.3031
gross reimbursed
vs
NADAC / ea
$0.2690
acquisition cost
=
Spread
+$1.0341
+384% 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 ⓘ
47% FFS 53% MCO
Fee-for-service · 2,759 Rx Managed care · 3,072 Rx
State Medicaid map
Alaska: 246 units · 33.6 per 100k residents AK Maine: no data reported ME Washington: 6,984 units · 89.4 per 100k residents WA Idaho: 838 units · 42.7 per 100k residents ID Montana: 3,050 units · 269 per 100k residents MT North Dakota: no data reported ND Minnesota: 5,889 units · 103 per 100k residents MN Wisconsin: 3,260 units · 55.2 per 100k residents WI Michigan: 2,738 units · 27.3 per 100k residents MI New York: 33,494 units · 171 per 100k residents NY Vermont: no data reported VT New Hampshire: 212 units · 15.1 per 100k residents NH Oregon: 7,652 units · 181 per 100k residents OR Nevada: no data reported NV Wyoming: no data reported WY South Dakota: no data reported SD Iowa: 594 units · 18.5 per 100k residents IA Illinois: 7,996 units · 63.7 per 100k residents IL Indiana: no data reported IN Ohio: 4,091 units · 34.7 per 100k residents OH Pennsylvania: 2,896 units · 22.3 per 100k residents PA New Jersey: 3,509 units · 37.8 per 100k residents NJ Massachusetts: 1,929 units · 27.6 per 100k residents MA California: 6,116 units · 15.7 per 100k residents CA Utah: 1,024 units · 30.0 per 100k residents UT Colorado: 3,766 units · 64.1 per 100k residents CO Nebraska: 1,333 units · 67.4 per 100k residents NE Missouri: 2,414 units · 39.0 per 100k residents MO Kentucky: 872 units · 19.3 per 100k residents KY West Virginia: no data reported WV Virginia: 884 units · 10.1 per 100k residents VA Maryland: 3,980 units · 64.4 per 100k residents MD Connecticut: 3,225 units · 89.2 per 100k residents CT Rhode Island: no data reported RI Arizona: 3,323 units · 44.7 per 100k residents AZ New Mexico: 4,899 units · 232 per 100k residents NM Kansas: no data reported KS Arkansas: no data reported AR Tennessee: no data reported TN North Carolina: 3,892 units · 35.9 per 100k residents NC South Carolina: no data reported SC Delaware: no data reported DE Oklahoma: 1,620 units · 40.0 per 100k residents OK Louisiana: 296 units · 6.5 per 100k residents LA Mississippi: no data reported MS Alabama: 916 units · 17.9 per 100k residents AL Georgia: no data reported GA D.C.: 2,051 units · 302 per 100k residents DC Hawaii: 326 units · 22.7 per 100k residents HI Texas: 927 units · 3.0 per 100k residents TX Florida: no data reported FL
Units reimbursed · per 100k residents
3.0302
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 D.C. 302 /100k
2 Montana 269 /100k
3 New Mexico 232 /100k
4 Oregon 181 /100k
5 New York 171 /100k
6 Minnesota 103 /100k
7 Washington 89.4 /100k
8 Connecticut 89.2 /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.

Medicaid utilization by pack size

Medicaid (SDUD) totals over the four most recent reported quarters for every package size of this drug — handy when a specific package (e.g. a starter/titration pack) carries little or no Medicaid volume on its own.
100 capsules16714-0388-02 6,723 Rx · $101,999
50 capsules this page16714-0388-01 5,831 Rx · $165,809
Drug total (last 4 qtrs): 12,554 Rx · 270,972 units · $267,808 gross reimbursed
Tap a pack size to open its page. Source: CMS State Drug Utilization Data, last 4 quarters.

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

Medicare Part D (outpatient prescription) spending for Cefadroxil — the program that covers self-administered drugs. 5 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 Cefadroxil. 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
$2.21M
Claims incl. refills
149.5K
Beneficiaries
130.4K
Spend / beneficiary
$16.92
Spend / claim
$14.76
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.

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Cefadroxil — the ingredient across all brands.

Top reported reactions

Pain355
Pneumonia278
Drug Hypersensitivity277
Dyspnoea270
Vomiting265
Asthma251
Cough241

Reporter sex

1,980 reports
Male · 34%
Female · 66%
Unknown · 0%

Serious outcomes

Death127
Disabling43
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 199 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
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.