NDC 68382-444

Famotidine 40 mg per 5 mL powder, for suspension

On the label: Zydus Pharmaceuticals (USA) Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Apothecon Pharmaceuticals Private LimitedVadodara, IndiaMakes it, tests it and packages it Problems found, fixed voluntarilyJan 27, 2023 · 3 inspections

Product details

Generic drug
Famotidine: every company that makes it
Form
powder, for suspension, oral
Strength
40 mg per 5 mL
Approval
ANDA ANDA091020
On the market since
Apr 22, 2021
Package NDCs
68382-444-05
Official label
DailyMed (National Library of Medicine), updated Dec 2, 2022

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