NDC 71205-277 – Ezetimibe

Ezetimibe 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-277

Product details

Brand name
Ezetimibe
Generic name
Ezetimibe
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209234
Marketed since
December 23, 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
71205-277-3030 TABLET in 1 BOTTLE (71205-277-30)May 1, 2019
71205-277-6060 TABLET in 1 BOTTLE (71205-277-60)May 1, 2019
71205-277-9090 TABLET in 1 BOTTLE (71205-277-90)May 1, 2019

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