NDC 63187-164
Sumatriptan 25 mg tablet
On the label: Proficient Rx LP. It's repackaged from NDC 63304-097, made by Sun Pharmaceutical Industries, Inc. (Sumatriptan). 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 (it lists 1 site that repackages it and relabels it). 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 Proficient Rx LP names for other drugs.
Product details
- Generic drug
- Sumatriptan: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA076554
- On the market since
- Aug 13, 2009
- Package NDCs
63187-164-09- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?