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
- 43063-696_4147b115-910a-13aa-e063-6394a90ad9e9
- Product NDC
- 43063-696
- Form
- TABLET
- Composition / generic term
- Famotidine
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20010416
- Source listing expiry
- 20261231
Source-listed ingredients
- FAMOTIDINE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-696-30) · 43063-696-30
- 90 TABLET in 1 BOTTLE, PLASTIC (43063-696-90) · 43063-696-90
- 180 TABLET in 1 BOTTLE, PLASTIC (43063-696-93) · 43063-696-93
- 1000 TABLET in 1 BOTTLE, PLASTIC (43063-696-95) · 43063-696-95
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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