NDC 60687-738 – Sucralfate

Sucralfate 1 g/10mL · Suspension · Oral

Human Prescription Drug

Product NDC60687-738

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
American Health Packaging
Dosage form
Suspension
Route
Oral
Marketing category
ANDA · ANDA211884
Marketed since
August 1, 2023
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
60687-738-083 TRAY in 1 CASE (60687-738-08) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-738-48) / 10 mL in 1 CUP, UNIT-DOSE (60687-738-42)Aug 1, 2023
60687-738-234 TRAY in 1 CASE (60687-738-23) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-738-48) / 10 mL in 1 CUP, UNIT-DOSE (60687-738-42)Aug 1, 2023
60687-738-5610 TRAY in 1 CASE (60687-738-56) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-738-48) / 10 mL in 1 CUP, UNIT-DOSE (60687-738-42)Aug 1, 2023

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