NDC 69238-1656 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC69238-1656

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA215576
Marketed since
April 22, 2022
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
69238-1656-1100 TABLET in 1 BOTTLE (69238-1656-1)Apr 22, 2022
69238-1656-5500 TABLET in 1 BOTTLE (69238-1656-5)May 23, 2022

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