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
- 68071-2306_1d785fd9-da03-92dd-e063-6294a90a9c1a
- Product NDC
- 68071-2306
- Form
- TABLET
- Composition / generic term
- Famotidine
- Labeler
- NuCare Pharmaceuticals,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
- 30 TABLET in 1 BOTTLE (68071-2306-3) · 68071-2306-3
- 180 TABLET in 1 BOTTLE (68071-2306-8) · 68071-2306-8
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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