NDC 68071-3478 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3478

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
NuCare Pharmaceuticals,Inc.
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 (1)

Package NDCDescriptionSince
68071-3478-330 TABLET in 1 BOTTLE, PLASTIC (68071-3478-3)Aug 3, 2023

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