NDC 16714-813 – Ezetimibe

Ezetimibe 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC16714-813

Product details

Brand name
Ezetimibe
Generic name
Ezetimibe
Labeler
NorthStar Rx LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209838
Marketed since
February 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Dietary Cholesterol Absorption Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Ezetimibe →

Package NDC codes (3)

Package NDCDescriptionSince
16714-813-0130 TABLET in 1 BOTTLE (16714-813-01)Feb 1, 2021
16714-813-0290 TABLET in 1 BOTTLE (16714-813-02)Feb 1, 2021
16714-813-03500 TABLET in 1 BOTTLE (16714-813-03)Feb 1, 2021

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