NDC 21695-546
Amoxicillin and Clavulanate Potassium 57 mg per 5 mL / 400 mg per 5 mL powder, for suspension
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Sandoz Inc.'s NDC 0781-6104.
Where the pills inside were 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
- Strength
- 57 mg per 5 mL / 400 mg per 5 mL
- Approval
- ANDA ANDA065066
- On the market since
- Jun 5, 2002
- Package NDCs
21695-546-00- Official label
- DailyMed (National Library of Medicine), updated Sep 14, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?