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
- 71335-1520_fd9976bd-f0c4-4e3a-b38b-2674f6e73c80
- Product NDC
- 71335-1520
- Form
- TABLET
- Composition / generic term
- Famotidine
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20010416
- Source listing expiry
- 20261231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-1520-1) · 71335-1520-1
- 60 TABLET in 1 BOTTLE (71335-1520-2) · 71335-1520-2
- 20 TABLET in 1 BOTTLE (71335-1520-3) · 71335-1520-3
- 90 TABLET in 1 BOTTLE (71335-1520-4) · 71335-1520-4
- 100 TABLET in 1 BOTTLE (71335-1520-5) · 71335-1520-5
- 10 TABLET in 1 BOTTLE (71335-1520-6) · 71335-1520-6
- 120 TABLET in 1 BOTTLE (71335-1520-7) · 71335-1520-7
- 50 TABLET in 1 BOTTLE (71335-1520-8) · 71335-1520-8
- 14 TABLET in 1 BOTTLE (71335-1520-9) · 71335-1520-9
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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