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
- 65162-062_71ed86a3-ff8a-4545-9bae-26632466fd80
- Product NDC
- 65162-062
- Form
- SUSPENSION
- Composition / generic term
- Sucralfate Oral
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191202
- 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 (65162-062-05) · 65162-062-05
- 10 CUP, UNIT-DOSE in 1 TRAY (65162-062-48) / 10 mL in 1 CUP, UNIT-DOSE (65162-062-47) · 65162-062-48
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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