United States · FDA National Drug Code directory
Sucralfate
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
- 59762-0401_311db6f8-1bc9-46af-a866-d7ad4d8193dc
- Product NDC
- 59762-0401
- Form
- TABLET
- Composition / generic term
- Sucralfate
- Labeler
- Mylan Pharmaceuticals, Inc.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20170925
- Source listing expiry
- 20271231
Source-listed ingredients
- SUCRALFATE — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (59762-0401-1) · 59762-0401-1
- 500 TABLET in 1 BOTTLE (59762-0401-5) · 59762-0401-5
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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