United States · FDA National Drug Code directory
Cimetidine
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
- 0378-0372_e8d57056-b0e8-4d9b-a239-1c3fe27d875e
- Product NDC
- 0378-0372
- Form
- TABLET, FILM COATED
- Composition / generic term
- cimetidine
- Labeler
- Mylan Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19940517
- Source listing expiry
- 20271231
Source-listed ingredients
- CIMETIDINE — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0372-01) · 0378-0372-01
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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