NDC 0121-0974 – Sucralfate

Sucralfate 1 g/10mL · Suspension · Oral

Human Prescription Drug

Product NDC0121-0974

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
Suspension
Route
Oral
Marketing category
ANDA · ANDA211884
Marketed since
March 15, 2022
Listing expires
December 31, 2027
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (4)

Package NDCDescriptionSince
0121-0974-0010 TRAY in 1 TRAY (0121-0974-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-0974-10)Aug 31, 2022
0121-0974-404 TRAY in 1 CASE (0121-0974-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-0974-10)Aug 31, 2022
0121-0974-505 PACKAGE in 1 TRAY (0121-0974-50) / 10 CUP, UNIT-DOSE in 1 PACKAGE / 10 mL in 1 CUP, UNIT-DOSE (0121-0974-10)Aug 31, 2022
0121-0974-943 TRAY in 1 CASE (0121-0974-94) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-0974-10)Aug 31, 2022

Other Sucralfate products