NDC 68071-3521

Famotidine 40 mg tablet, film coated

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 70710-1684.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections

Repackaging site

Product details

Generic drug
Famotidine: every company that makes it
Form
tablet, film coated, oral
Strength
40 mg
Approval
ANDA ANDA216441
On the market since
Jun 6, 2022
Package NDCs
68071-3521-3
Official label
DailyMed (National Library of Medicine), updated Feb 3, 2025

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