NDC 72189-234 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC72189-234

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
DIRECT RX
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA070848
Marketed since
June 18, 2021
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
72189-234-2020 TABLET in 1 BOTTLE (72189-234-20)Jun 18, 2021
72189-234-9090 TABLET in 1 BOTTLE (72189-234-90)Jun 18, 2021

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