NDC 80425-0091 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC80425-0091

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA070848
Marketed since
November 11, 1996
Listing expires
December 31, 2026
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (1)

Package NDCDescriptionSince
80425-0091-130 TABLET in 1 BOTTLE (80425-0091-1)Nov 11, 1996

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