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
- 72865-215_b37fe9a5-6465-4518-823d-5d369a4c7793
- Product NDC
- 72865-215
- Form
- TABLET, FILM COATED
- Composition / generic term
- Famotidine
- Labeler
- XLCare Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211015
- Source listing expiry
- 20261231
Source-listed ingredients
- FAMOTIDINE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (72865-215-01) · 72865-215-01
- 500 TABLET, FILM COATED in 1 BOTTLE (72865-215-05) · 72865-215-05
- 180 TABLET, FILM COATED in 1 BOTTLE (72865-215-18) · 72865-215-18
- 30 TABLET, FILM COATED in 1 BOTTLE (72865-215-30) · 72865-215-30
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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