NDC 82804-064 – Ezetimibe

Ezetimibe 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-064

Product details

Brand name
Ezetimibe
Generic name
Ezetimibe
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209838
Marketed since
August 25, 2017
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
82804-064-3030 TABLET in 1 BOTTLE (82804-064-30)Jan 31, 2024
82804-064-6060 TABLET in 1 BOTTLE (82804-064-60)Jan 31, 2024
82804-064-9090 TABLET in 1 BOTTLE (82804-064-90)Jan 31, 2024

Other Ezetimibe products