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
- 0713-0791_27c19a55-ceb8-91c3-e063-6394a90a726e
- Product NDC
- 0713-0791
- Form
- SUSPENSION
- Composition / generic term
- Sucralfate
- Labeler
- Cosette Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241219
- Source listing expiry
- 20261231
Source-listed ingredients
- SUCRALFATE — 1 g/10mL
These values do not establish equivalence or a dose recommendation.
Packages
- 420 mL in 1 BOTTLE (0713-0791-75) · 0713-0791-75
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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