NDC 16714-781 – Ezetimibe and simvastatin

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

Human Prescription Drug

Product NDC16714-781

Product details

Brand name
Ezetimibe and simvastatin
Generic name
Ezetimibe and simvastatin
Labeler
NORTHSTAR RX LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208699
Marketed since
August 19, 2019
Marketing end
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 (2)

Package NDCDescriptionSince
16714-781-0130 TABLET in 1 BOTTLE (16714-781-01)Aug 19, 2019
16714-781-0290 TABLET in 1 BOTTLE (16714-781-02)Aug 19, 2019

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