NDC 70771-1833 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC70771-1833

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA215705
Marketed since
May 20, 2023
Listing expires
December 31, 2027
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (3)

Package NDCDescriptionSince
70771-1833-1100 TABLET in 1 BOTTLE (70771-1833-1)May 20, 2023
70771-1833-330 TABLET in 1 BOTTLE (70771-1833-3)May 20, 2023
70771-1833-5500 TABLET in 1 BOTTLE (70771-1833-5)May 20, 2023

Other Sucralfate products