Quick answers
- What is Amoxicillin/Clav Pot?
- Amoxicillin/Clav Pot is a brand name of Amoxicillin and clavulanate potassium (amoxicillin / clavulanate), a prescription medicine. The FDA NDC Directory lists 1 Amoxicillin/Clav Pot product in 1 strength and form.
- Who makes Amoxicillin/Clav Pot?
- Micro Labs Ltd India holds the FDA application for Amoxicillin/Clav Pot (ANDA205707, approved December 30, 2016).
- Is there a generic or store brand of Amoxicillin/Clav Pot?
- Yes. The FDA NDC Directory lists 36 other products with the same active ingredients, strength and form as a Amoxicillin/Clav Pot product, 36 of them generic. Ask your pharmacist whether one is right for you.
- Has Amoxicillin/Clav Pot been recalled?
- No recall linked to Amoxicillin/Clav Pot products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Amoxicillin/Clav Pot is
Each Amoxicillin/Clav Pot 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 500 mg · clavulanate potassium 125 mg tablet, film coated (oral) | Amoxicillin/Clav Pot | 36 products, 19 companies | DailyMed |
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
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA205707 | Micro Labs Ltd India | December 30, 2016 | 1 |
Companies that list Amoxicillin/Clav Pot
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Amoxicillin/Clav Pot products.
- Direct_Rx1 product
Recalls
No recall linked to Amoxicillin/Clav Pot 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.