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
63629-9152_68eb54fd-5a5e-4803-a43e-1c3134416377
Product NDC
63629-9152
Form
TABLET
Composition / generic term
Sucralfate
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20200217
Source listing expiry
20261231

Source-listed ingredients

  • SUCRALFATE — 1 g/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE, PLASTIC (63629-9152-1) · 63629-9152-1

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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