NDC 0781-6102
Amoxicillin and Clavulanate Potassium 200 mg per 5 mL / 28.5 mg per 5 mL powder, for suspension
On the label: Sandoz 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 Sandoz Inc. names for other drugs.
Recalls
- Apr 26, 2017 · Class III · Sandoz Inc
Subpotent Drug; Clavulanic Acid
Lots: Lot FP8735, 8/2017
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 ANDA065066
- On the market since
- Jun 5, 2002
- Package NDCs
0781-6102-460781-6102-520781-6102-57- Official label
- DailyMed (National Library of Medicine), updated May 1, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?