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
- 71335-0409_d24aad6a-0ce6-45d1-a84a-2e738c497bb2
- Product NDC
- 71335-0409
- Form
- TABLET
- Composition / generic term
- Famotidine
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160129
- Source listing expiry
- 20271231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 40 TABLET in 1 BOTTLE (71335-0409-0) · 71335-0409-0
- 30 TABLET in 1 BOTTLE (71335-0409-1) · 71335-0409-1
- 60 TABLET in 1 BOTTLE (71335-0409-2) · 71335-0409-2
- 20 TABLET in 1 BOTTLE (71335-0409-3) · 71335-0409-3
- 90 TABLET in 1 BOTTLE (71335-0409-4) · 71335-0409-4
- 100 TABLET in 1 BOTTLE (71335-0409-5) · 71335-0409-5
- 10 TABLET in 1 BOTTLE (71335-0409-6) · 71335-0409-6
- 120 TABLET in 1 BOTTLE (71335-0409-7) · 71335-0409-7
- 50 TABLET in 1 BOTTLE (71335-0409-8) · 71335-0409-8
- 14 TABLET in 1 BOTTLE (71335-0409-9) · 71335-0409-9
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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