Quick answers
- What is Augmentin?
- Augmentin is a brand name of Amoxicillin and clavulanate potassium (amoxicillin / clavulanate), a prescription medicine. The FDA NDC Directory lists 1 Augmentin product in 1 strength and form.
- Who makes Augmentin?
- US Antibiotics holds the FDA application for Augmentin (NDA050575, approved August 6, 1984).
- Is there a generic or store brand of Augmentin?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Augmentin product, 1 of them generic. Ask your pharmacist whether one is right for you.
- Has Augmentin been recalled?
- No recall linked to Augmentin products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Augmentin is
Each Augmentin product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Amoxicillin and clavulanate potassium (amoxicillin / clavulanate) · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| amoxicillin 125 mg/5 mL · clavulanate potassium 31.25 mg/5 mL for suspension (oral) | Augmentin | 1 product, 1 company | — |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Amoxicillin and clavulanate potassium (amoxicillin / clavulanate) →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA050575 | US Antibiotics | August 6, 1984 | 1 |
Companies that list Augmentin
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Augmentin products.
- Allegis Holdings, LLC1 product
Recalls
No recall linked to Augmentin products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.