NDC 43598-742 – Ezetimibe and Simvastatin

Ezetimibe 10 mg/1; Simvastatin 10 mg/1 · Tablet · Oral

Human Prescription Drug 5 recalls

Product NDC43598-742

Product details

Brand name
Ezetimibe and Simvastatin
Generic name
Ezetimibe and Simvastatin
Labeler
Dr.Reddys Laboratories Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA200909
Marketed since
November 20, 2018
Marketing end
October 31, 2027
Pharmacologic class
Dietary Cholesterol Absorption Inhibitor; HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for ezetimibe and simvastatin →

Package NDC codes (3)

Package NDCDescriptionSince
43598-742-101000 TABLET in 1 BOTTLE (43598-742-10)Nov 20, 2018
43598-742-3030 TABLET in 1 BOTTLE (43598-742-30)Nov 20, 2018
43598-742-9090 TABLET in 1 BOTTLE (43598-742-90)Nov 20, 2018

Recalls mentioning this NDC

Other ezetimibe and simvastatin products