Zetia - 54569-5489-0 - (Ezetimibe)

Alphabetical Index


Drug Information of Zetia

Product NDC: 54569-5489
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: 54569-5489
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021445
Marketing Category: NDA
Start Marketing Date: 20090727

Package Information of Zetia

Package NDC: 54569-5489-0
Package Description: 30 TABLET in 1 BOTTLE, DISPENSING (54569-5489-0)

NDC Information of Zetia

NDC Code 54569-5489-0
Proprietary Name Zetia
Package Description 30 TABLET in 1 BOTTLE, DISPENSING (54569-5489-0)
Product NDC 54569-5489
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 A-S Medication Solutions LLC
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