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
- 71335-2637_dc7f253b-f40a-4774-8456-1d383fb35b0c
- Product NDC
- 71335-2637
- Form
- TABLET
- Composition / generic term
- Sucralfate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20170925
- Source listing expiry
- 20261231
Source-listed ingredients
- SUCRALFATE — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 28 TABLET in 1 BOTTLE (71335-2637-0) · 71335-2637-0
- 100 TABLET in 1 BOTTLE (71335-2637-1) · 71335-2637-1
- 60 TABLET in 1 BOTTLE (71335-2637-2) · 71335-2637-2
- 30 TABLET in 1 BOTTLE (71335-2637-3) · 71335-2637-3
- 20 TABLET in 1 BOTTLE (71335-2637-4) · 71335-2637-4
- 150 TABLET in 1 BOTTLE (71335-2637-6) · 71335-2637-6
- 90 TABLET in 1 BOTTLE (71335-2637-7) · 71335-2637-7
- 40 TABLET in 1 BOTTLE (71335-2637-8) · 71335-2637-8
- 120 TABLET in 1 BOTTLE (71335-2637-9) · 71335-2637-9
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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