NDC 82009-024 – ezetimibe

Ezetimibe 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82009-024

Product details

Brand name
ezetimibe
Generic name
ezetimibe
Labeler
Quallent Pharmaceuticals Health LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204331
Marketed since
August 20, 2022
Listing expires
December 31, 2026
Pharmacologic class
Dietary Cholesterol Absorption Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Ezetimibe →

Package NDC codes (1)

Package NDCDescriptionSince
82009-024-05500 TABLET in 1 BOTTLE (82009-024-05)Aug 20, 2022

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