NDC 68788-8316 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8316

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA018333
Marketed since
December 23, 2022
Listing expires
December 31, 2027
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (2)

Package NDCDescriptionSince
68788-8316-1100 TABLET in 1 BOTTLE (68788-8316-1)Dec 23, 2022
68788-8316-330 TABLET in 1 BOTTLE (68788-8316-3)Dec 23, 2022

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