NDC 51655-475 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-475

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA018333
Marketed since
November 18, 2020
Listing expires
December 31, 2027
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (1)

Package NDCDescriptionSince
51655-475-5230 TABLET in 1 BOTTLE, PLASTIC (51655-475-52)Nov 18, 2020

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