NDC 21695-767
Amoxicillin and Clavulanate Potassium 200 mg per 5 mL / 28.5 mg per 5 mL powder, for suspension
On the label: Rebel Distributors Corp... It's repackaged from NDC 66685-1011, made by Sandoz Inc (Amoxicillin and Clavulanate Potassium). That product's FDA listing has since ended, so its label and factories are no longer published.
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 Rebel Distributors Corp.. names for other drugs.
Product details
- Generic drug
- Amoxicillin and Clavulanic Acid: every company that makes it
- Form
- powder, for suspension
- Strength
- 200 mg per 5 mL / 28.5 mg per 5 mL
- Approval
- ANDA ANDA065066
- On the market since
- Jun 5, 2002
- Package NDCs
21695-767-50- Official label
- DailyMed (National Library of Medicine), updated Jul 20, 2011
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