NDC 68788-8946 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8946

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA070848
Marketed since
October 27, 2015
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
68788-8946-1100 TABLET in 1 BOTTLE (68788-8946-1)Oct 28, 2015
68788-8946-330 TABLET in 1 BOTTLE (68788-8946-3)Oct 28, 2015

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