NDC 71610-017 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-017

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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 (3)

Package NDCDescriptionSince
71610-017-6090 TABLET in 1 BOTTLE (71610-017-60)Dec 27, 2017
71610-017-70120 TABLET in 1 BOTTLE (71610-017-70)Jan 19, 2018
71610-017-94360 TABLET in 1 BOTTLE (71610-017-94)Jan 19, 2018

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