NDC 0093-2277
Amoxicillin and Clavulanate Potassium 200 mg per 5 mL / 28.5 mg per 5 mL powder, for suspension
On the label: Teva Pharmaceuticals USA, Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.
Recalls
- Oct 13, 2025 · Class II · Teva Pharmaceuticals USA, Inc
Subpotent drug; Clavulanate Potassium component
Lots: Lot # 100062316, Exp Date: 01/2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Amoxicillin and Clavulanic Acid: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 200 mg per 5 mL / 28.5 mg per 5 mL
- Approval
- ANDA ANDA065089
- On the market since
- Jan 13, 2005
- Package NDCs
0093-2277-73- Official label
- DailyMed (National Library of Medicine), updated Jun 1, 2024
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