NDC 50436-4623

Sumatriptan 50 mg tablet

On the label: Unit Dose Services. It's a repackaged product (source NDC 63304-098, which isn't on a current label).

Where it's made

This label doesn't name the factory that makes the drug (it lists 1 site that repackages it and relabels it). Companies aren't required to print it on the label. The manufacturer's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Unit Dose Services uses for other drugs.

Product details

Generic drug

Sumatriptan: see every company that makes it

Form

tablet

Strength

50 mg

Approval

ANDA ANDA076554

On the market since

Aug 13, 2009

Package NDCs

50436-4623-1

Official label

DailyMed (National Library of Medicine), updated Jul 1, 2017

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?