NDC 17856-0306 – Sucralfate

Sucralfate 1 g/10mL · Suspension · Oral

Human Prescription Drug

Product NDC17856-0306

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
ATLANTIC BIOLOGICALS CORP.
Dosage form
Suspension
Route
Oral
Marketing category
ANDA · ANDA211884
Marketed since
March 15, 2022
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
17856-0306-172 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0306-1) / 10 mL in 1 CUP, UNIT-DOSEAug 10, 2023

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