United States · FDA National Drug Code directory

maximum strength

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
56062-194_106cff2c-1d3b-4f5d-ab79-5f67e04594d6
Product NDC
56062-194
Form
TABLET, FILM COATED
Composition / generic term
Famotidine
Labeler
Publix Super Markets Inc
Marketing category
ANDA
Marketing start / end (source format)
20071203
Source listing expiry
20261231

Source-listed ingredients

  • FAMOTIDINE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 25 BLISTER PACK in 1 CARTON (56062-194-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK · 56062-194-02
  • 1 BOTTLE in 1 CARTON (56062-194-71) / 50 TABLET, FILM COATED in 1 BOTTLE · 56062-194-71

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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