NDC 51660-200 – Ezetimibe

Ezetimibe 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51660-200

Product details

Brand name
Ezetimibe
Generic name
Ezetimibe
Labeler
Ohm Laboratories Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207311
Marketed since
June 12, 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
51660-200-05500 TABLET in 1 BOTTLE (51660-200-05)Jun 12, 2017
51660-200-3030 TABLET in 1 BOTTLE (51660-200-30)Jun 12, 2017
51660-200-9090 TABLET in 1 BOTTLE (51660-200-90)Jun 12, 2017

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