NDC 50436-0319

Ibuprofen 400 mg tablet, film coated

On the label: Unit Dose Services. It's a repackaged product: Unit Dose Services rebottles it from Ascend Laboratories, LLC's NDC 67877-319.

Where the pills inside were made

Granules India Limited

Medchal-Malkajgiri District, India · makes it, tests it and packages it

Problems found, fixed voluntarily Last FDA inspection Feb 14, 2020. 6 inspections on record.

Repackaging site

Product details

Generic drug
Ibuprofen: see every company that makes it
Form
tablet, film coated
Strength
400 mg
Approval
ANDA ANDA091625
On the market since
Dec 21, 2015
Package NDCs
50436-0319-1 50436-0319-6 50436-0319-7
Official label
DailyMed (National Library of Medicine), updated Aug 24, 2021

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