NDC 71335-2637 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2637

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA018333
Marketed since
September 25, 2017
Listing expires
December 31, 2026
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (9)

Package NDCDescriptionSince
71335-2637-028 TABLET in 1 BOTTLE (71335-2637-0)Jun 2, 2025
71335-2637-1100 TABLET in 1 BOTTLE (71335-2637-1)Jun 2, 2025
71335-2637-260 TABLET in 1 BOTTLE (71335-2637-2)Jun 2, 2025
71335-2637-330 TABLET in 1 BOTTLE (71335-2637-3)Jun 2, 2025
71335-2637-420 TABLET in 1 BOTTLE (71335-2637-4)Jun 2, 2025
71335-2637-6150 TABLET in 1 BOTTLE (71335-2637-6)Jun 2, 2025
71335-2637-790 TABLET in 1 BOTTLE (71335-2637-7)Jun 2, 2025
71335-2637-840 TABLET in 1 BOTTLE (71335-2637-8)Jun 2, 2025
71335-2637-9120 TABLET in 1 BOTTLE (71335-2637-9)Jun 2, 2025

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