NDC 81033-149 – Sucralfate

Sucralfate 1 g/10mL · Suspension · Oral

Human Prescription Drug

Product NDC81033-149

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Kesin Pharma Corporation
Dosage form
Suspension
Route
Oral
Marketing category
ANDA · ANDA216474
Marketed since
July 1, 2024
Listing expires
December 31, 2026
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (2)

Package NDCDescriptionSince
81033-149-4440 CUP, UNIT-DOSE in 1 CARTON (81033-149-44) / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10)Jul 1, 2024
81033-149-52100 CUP, UNIT-DOSE in 1 CASE (81033-149-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10)Jul 1, 2024

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