NDC 66116-413
Sumatriptan Succinate 50 mg tablet, film coated
On the label: MedVantx, Inc.. It's repackaged from NDC 0093-0223, made by Teva Pharmaceuticals USA Inc (Sumatriptan Succinate). 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 MedVantx, Inc. names for other drugs.
Product details
- Generic drug
- Sumatriptan: every company that makes it
- Form
- tablet, film coated
- Strength
- 50 mg
- Approval
- ANDA ANDA076840
- On the market since
- Sep 22, 2010
- Package NDCs
66116-413-09- Official label
- DailyMed (National Library of Medicine), updated Sep 22, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?