NDC 21695-384
Amoxicillin 125 mg per 5 mL powder, for suspension
On the label: Rebel Distributors Corp... It's repackaged from NDC 0093-4150, made by Teva Pharmaceuticals USA, Inc. (Amoxicillin). 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: every company that makes it
- Form
- powder, for suspension
- Strength
- 125 mg per 5 mL
- Approval
- ANDA ANDA061931
- On the market since
- Feb 1, 2010
- Package NDCs
21695-384-1521695-384-80- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2010
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