NDC 58914-171 – Carafate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC58914-171

Product details

Brand name
Carafate
Generic name
Sucralfate
Labeler
Allergan, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA018333
Marketed since
October 30, 1981
Listing expires
December 31, 2026
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Carafate →

Package NDC codes (1)

Package NDCDescriptionSince
58914-171-10100 TABLET in 1 BOTTLE (58914-171-10)Oct 30, 1981

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