Zetia - 21695-778-90 - (Ezetimibe)

Alphabetical Index


Drug Information of Zetia

Product NDC: 21695-778
Proprietary Name: Zetia
Non Proprietary Name: Ezetimibe
Active Ingredient(s): 10    mg/1 & nbsp;   Ezetimibe
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Zetia

Product NDC: 21695-778
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021445
Marketing Category: NDA
Start Marketing Date: 20090727

Package Information of Zetia

Package NDC: 21695-778-90
Package Description: 90 TABLET in 1 BOTTLE (21695-778-90)

NDC Information of Zetia

NDC Code 21695-778-90
Proprietary Name Zetia
Package Description 90 TABLET in 1 BOTTLE (21695-778-90)
Product NDC 21695-778
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ezetimibe
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090727
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
Substance Name EZETIMIBE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Decreased Cholesterol Absorption [PE],Dietary Cholesterol Absorption Inhibitor [EPC]

Complete Information of Zetia


General Information