NDC 70954-316

Famotidine 40 mg per 5 mL powder, for suspension

On the label: ANI Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Novitium Pharma LLCEast Windsor, NJ, United StatesMakes it, tests it, packages it and labels it No problems foundFeb 16, 2024 · 5 inspections

Product details

Generic drug
Famotidine: every company that makes it
Form
powder, for suspension, oral
Strength
40 mg per 5 mL
Approval
ANDA ANDA215043
On the market since
Apr 20, 2021
Package NDCs
70954-316-10
Official label
DailyMed (National Library of Medicine), updated Oct 2, 2023

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