NDC 82804-211 – Ezetimibe

Ezetimibe 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-211

Product details

Brand name
Ezetimibe
Generic name
Ezetimibe
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078560
Marketed since
April 29, 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
82804-211-3030 TABLET in 1 BOTTLE (82804-211-30)Mar 19, 2025

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