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
- 63629-1307_fc785200-389b-e031-e053-6294a90a88f1
- Product NDC
- 63629-1307
- Form
- TABLET
- Composition / generic term
- Sucralfate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19961111
- 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 (63629-1307-0) · 63629-1307-0
- 100 TABLET in 1 BOTTLE (63629-1307-1) · 63629-1307-1
- 60 TABLET in 1 BOTTLE (63629-1307-2) · 63629-1307-2
- 30 TABLET in 1 BOTTLE (63629-1307-3) · 63629-1307-3
- 20 TABLET in 1 BOTTLE (63629-1307-4) · 63629-1307-4
- 150 TABLET in 1 BOTTLE (63629-1307-6) · 63629-1307-6
- 90 TABLET in 1 BOTTLE (63629-1307-7) · 63629-1307-7
- 40 TABLET in 1 BOTTLE (63629-1307-8) · 63629-1307-8
- 120 TABLET in 1 BOTTLE (63629-1307-9) · 63629-1307-9
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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