NDC 67877-510 – Ezetimibe and Simvastatin

Ezetimibe 10 mg/1; Simvastatin 80 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC67877-510

Product details

Brand name
Ezetimibe and Simvastatin
Generic name
Ezetimibe and Simvastatin
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209222
Marketed since
December 24, 2017
Listing expires
December 31, 2026
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 (4)

Package NDCDescriptionSince
67877-510-05500 TABLET in 1 BOTTLE (67877-510-05)Dec 24, 2017
67877-510-3030 TABLET in 1 BOTTLE (67877-510-30)Dec 24, 2017
67877-510-375 BLISTER PACK in 1 CARTON (67877-510-37) / 10 TABLET in 1 BLISTER PACK (67877-510-33)Dec 24, 2017
67877-510-9090 TABLET in 1 BOTTLE (67877-510-90)Dec 24, 2017

Other Ezetimibe and simvastatin products