NDC 72162-2264 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-2264

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074415
Marketed since
February 17, 2020
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
72162-2264-1100 TABLET in 1 BOTTLE, PLASTIC (72162-2264-1)Feb 23, 2024
72162-2264-5500 TABLET in 1 BOTTLE, PLASTIC (72162-2264-5)Feb 23, 2024

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