NDC 66689-305 – Sucralfate

Sucralfate 1 g/10mL · Suspension · Oral

Human Prescription Drug 2 recalls

Product NDC66689-305

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
VistaPharm, LLC
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 (1)

Package NDCDescriptionSince
66689-305-161 BOTTLE, PLASTIC in 1 CARTON (66689-305-16) / 414 mL in 1 BOTTLE, PLASTICMar 15, 2022

Recalls mentioning this NDC

Other Sucralfate products