NDC 80425-0329

Famotidine 20 mg tablet, film coated

On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged: Advanced Rx Pharmacy of Tennessee, LLC rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-017.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Annora Pharma Private LimitedSangareddy, IndiaMakes it and tests it Problems found, fixed voluntarilyMar 28, 2025 · 4 inspections

Repackaging site

Product details

Generic drug
Famotidine: every company that makes it
Form
tablet, film coated, oral
Strength
20 mg
Approval
ANDA ANDA215767
On the market since
Apr 24, 2023
Package NDCs
80425-0329-1 80425-0329-2 80425-0329-3
Official label
DailyMed (National Library of Medicine), updated Dec 31, 2024

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