United States · FDA National Drug Code directory

acid controller

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
0363-1203_a781400e-15a6-4d62-abb7-c92680a18e51
Product NDC
0363-1203
Form
TABLET, FILM COATED
Composition / generic term
famotidine
Labeler
Walgreen Company
Marketing category
ANDA
Marketing start / end (source format)
20220407
Source listing expiry
20271231

Source-listed ingredients

  • FAMOTIDINE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (0363-1203-71) / 50 TABLET, FILM COATED in 1 BOTTLE · 0363-1203-71

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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