NDC 53002-3199

Famotidine 20 mg tablet

On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Carlsbad Technology, Inc.'s NDC 61442-121.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Carlsbad Technology, Inc.Carlsbad, CA, United StatesMakes it Problems found, fixed voluntarilyJun 30, 2026 · 12 inspections
Carlsbad Technology, Inc.Carlsbad, CA, United StatesLabels it Problems found, fixed voluntarilyJun 30, 2026 · 12 inspections

Repackaging site

Product details

Generic drug
Famotidine: every company that makes it
Form
tablet
Strength
20 mg
Approval
ANDA ANDA075805
On the market since
Apr 16, 2001
Package NDCs
53002-3199-0 53002-3199-2 53002-3199-3 53002-3199-5 53002-3199-6
Official label
DailyMed (National Library of Medicine), updated Mar 30, 2022

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