United States · FDA National Drug Code directory

Famotidine

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 55154-4313_c2ae9c82-2f61-45df-977e-4f2e0f0d58e2
Product NDC: 55154-4313
Form: TABLET, FILM COATED
Composition / generic term: Famotidine
Labeler: Cardinal Health 107, LLC
Marketing category: ANDA
Marketing start / end (source format): 20010416
Source listing expiry: 20271231

Source-listed ingredients

FAMOTIDINE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

10 BLISTER PACK in 1 BAG (55154-4313-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK · 55154-4313-0

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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