NDC 72189-429 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC72189-429

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Direct_Rx
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074415
Marketed since
March 2, 2023
Listing expires
December 31, 2026
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (2)

Package NDCDescriptionSince
72189-429-2020 TABLET in 1 BOTTLE (72189-429-20)Mar 2, 2023
72189-429-9090 TABLET in 1 BOTTLE (72189-429-90)Mar 2, 2023

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