NDC 51655-031 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-031

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA070848
Marketed since
February 9, 2015
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
51655-031-5230 TABLET in 1 BOTTLE, DISPENSING (51655-031-52)Feb 9, 2015

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