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
- 59651-701_186342b3-2a01-4582-8978-41f059d4307d
- Product NDC
- 59651-701
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- FAMOTIDINE
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250709
- Source listing expiry
- 20271231
Source-listed ingredients
- FAMOTIDINE — 40 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 50 mL in 1 BOTTLE (59651-701-50) · 59651-701-50
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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