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FDA Drug information

Ezetimibe

Read time: 1 mins
Marketing start date: 03 May 2024

Summary of product characteristics


Effective Time

20220826

Version

4

Spl Product Data Elements

ezetimibe ezetimibe EZETIMIBE EZETIMIBE CELLULOSE, MICROCRYSTALLINE CROSPOVIDONE LACTOSE MONOHYDRATE MAGNESIUM STEARATE POVIDONE SODIUM LAURYL SULFATE SODIUM STEARYL FUMARATE STARCH, CORN WHITE TO OFF-WHITE CAPSULE 773

Application Number

ANDA204331

Brand Name

Ezetimibe

Generic Name

ezetimibe

Product Ndc

70771-1109

Product Type

HUMAN PRESCRIPTION DRUG

Route

ORAL

Package Label Principal Display Panel

NDC 70771-1109-3 in bottle of 30 tablets Ezetimibe Tablets , 10 mg Rx only 30 tablets Ezetimibe Tablets, 10 mg

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