NDC 71335-2114 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2114

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 (9)

Package NDCDescriptionSince
71335-2114-028 TABLET in 1 BOTTLE, PLASTIC (71335-2114-0)Jun 20, 2022
71335-2114-1100 TABLET in 1 BOTTLE, PLASTIC (71335-2114-1)Jun 20, 2022
71335-2114-260 TABLET in 1 BOTTLE, PLASTIC (71335-2114-2)Jun 20, 2022
71335-2114-330 TABLET in 1 BOTTLE, PLASTIC (71335-2114-3)Jun 20, 2022
71335-2114-420 TABLET in 1 BOTTLE, PLASTIC (71335-2114-4)Jun 20, 2022
71335-2114-6150 TABLET in 1 BOTTLE, PLASTIC (71335-2114-6)Jun 20, 2022
71335-2114-790 TABLET in 1 BOTTLE, PLASTIC (71335-2114-7)Jun 20, 2022
71335-2114-840 TABLET in 1 BOTTLE, PLASTIC (71335-2114-8)Jun 20, 2022
71335-2114-9120 TABLET in 1 BOTTLE, PLASTIC (71335-2114-9)Jun 20, 2022

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