NDC 50436-5996

benzonatate 200 mg capsule

On the label: Unit Dose Services. It's a repackaged product (source NDC 67877-106, 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

Benzonatate: see every company that makes it

Form

capsule

Strength

200 mg

Approval

ANDA ANDA040749

On the market since

Jul 25, 2007

Package NDCs

50436-5996-1

Official label

DailyMed (National Library of Medicine), updated Mar 6, 2017

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