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
- 67457-433_8845646e-1471-490d-a26b-f18c7e31a4c0
- Product NDC
- 67457-433
- Form
- INJECTION
- Composition / generic term
- Famotidine
- Labeler
- Mylan Institutional LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080626
- Source listing expiry
- 20271231
Source-listed ingredients
- FAMOTIDINE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 CARTON (67457-433-22) / 2 mL in 1 VIAL (67457-433-00) · 67457-433-22
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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