NDC 68788-8779 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8779

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Preferred Pharmaceuticals Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA215705
Marketed since
December 10, 2024
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
68788-8779-330 TABLET in 1 BOTTLE (68788-8779-3)Dec 10, 2024
68788-8779-9100 TABLET in 1 BOTTLE (68788-8779-9)Dec 10, 2024

Other Sucralfate products