NDC 31722-315

Ibuprofen And Famotidine 800 mg / 26.6 mg tablet

On the label: Camber Pharmaceuticals Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Ascent Pharmaceuticals IncCentral Islip, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections

Product details

Generic drug
Famotidine and Ibuprofen: every company that makes it
Form
tablet, oral
Strength
800 mg / 26.6 mg
Approval
ANDA ANDA216814
On the market since
Mar 15, 2023
Package NDCs
31722-315-90
Official label
DailyMed (National Library of Medicine), updated Jul 11, 2024

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