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
- 72205-145_34acb853-6632-49cd-970a-e6fd840852d3
- Product NDC
- 72205-145
- Form
- TABLET, FILM COATED
- Composition / generic term
- Famotidine
- Labeler
- Novadoz Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240806
- Source listing expiry
- 20261231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET, FILM COATED in 1 BOTTLE (72205-145-05) · 72205-145-05
- 30 TABLET, FILM COATED in 1 BOTTLE (72205-145-30) · 72205-145-30
- 50 TABLET, FILM COATED in 1 BOTTLE (72205-145-50) · 72205-145-50
- 100 TABLET, FILM COATED in 1 BOTTLE (72205-145-91) · 72205-145-91
- 75 TABLET, FILM COATED in 1 BOTTLE (72205-145-98) · 72205-145-98
- 1000 TABLET, FILM COATED in 1 BOTTLE (72205-145-99) · 72205-145-99
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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