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
- 51407-683_22941e23-59e9-f792-e063-6394a90a2552
- Product NDC
- 51407-683
- Form
- TABLET
- Composition / generic term
- Famotidine
- Labeler
- Golden State Medical Supply, Inc.
- 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
- 36 BOTTLE in 1 BOX (51407-683-10) / 1000 TABLET in 1 BOTTLE · 51407-683-10
- 36 BOTTLE in 1 BOX (51407-683-18) / 180 TABLET in 1 BOTTLE · 51407-683-18
- 36 BOTTLE in 1 BOX (51407-683-25) / 25 TABLET in 1 BOTTLE · 51407-683-25
- 36 BOTTLE in 1 BOX (51407-683-30) / 30 TABLET in 1 BOTTLE · 51407-683-30
- 36 BOTTLE in 1 BOX (51407-683-50) / 50 TABLET in 1 BOTTLE · 51407-683-50
- 36 BOTTLE in 1 BOX (51407-683-90) / 90 TABLET in 1 BOTTLE · 51407-683-90
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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