NDC 0713-0791 – Sucralfate

Sucralfate 1 g/10mL · Suspension · Oral

Human Prescription Drug

Product NDC0713-0791

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Cosette Pharmaceuticals, Inc.
Dosage form
Suspension
Route
Oral
Marketing category
ANDA · ANDA217126
Marketed since
December 19, 2024
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
0713-0791-75420 mL in 1 BOTTLE (0713-0791-75)Dec 19, 2024

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