NDC 50436-3138

Fosinopril Sodium 20 mg tablet

On the label: Unit Dose Services. It's a repackaged product (source NDC 31722-201, 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). 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

Fosinoprilat: see every company that makes it

Form

tablet

Strength

20 mg

Approval

ANDA ANDA077222

On the market since

Sep 17, 2007

Package NDCs

50436-3138-1

Official label

DailyMed (National Library of Medicine), updated Jan 25, 2011

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