NDC 71610-541 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-541

Product details

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

Package NDCDescriptionSince
71610-541-6090 TABLET in 1 BOTTLE, PLASTIC (71610-541-60)Apr 13, 2021
71610-541-70120 TABLET in 1 BOTTLE, PLASTIC (71610-541-70)Apr 13, 2021
71610-541-94360 TABLET in 1 BOTTLE, PLASTIC (71610-541-94)Apr 13, 2021

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