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
- 63187-723_c34993a0-b4e0-4443-a5b7-1fc9e2b019f7
- Product NDC
- 63187-723
- Form
- TABLET
- Composition / generic term
- Famotidine
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160129
- Source listing expiry
- 20261231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (63187-723-00) · 63187-723-00
- 6 TABLET in 1 BOTTLE (63187-723-06) · 63187-723-06
- 10 TABLET in 1 BOTTLE (63187-723-10) · 63187-723-10
- 30 TABLET in 1 BOTTLE (63187-723-30) · 63187-723-30
- 60 TABLET in 1 BOTTLE (63187-723-60) · 63187-723-60
- 90 TABLET in 1 BOTTLE (63187-723-90) · 63187-723-90
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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