Zetia - 66582-414-15 - (Ezetimibe)

Alphabetical Index


Drug Information of Zetia

Product NDC: 66582-414
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: 66582-414
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021445
Marketing Category: NDA
Start Marketing Date: 20021025

Package Information of Zetia

Package NDC: 66582-414-15
Package Description: 7 TABLET in 1 BLISTER PACK (66582-414-15)

NDC Information of Zetia

NDC Code 66582-414-15
Proprietary Name Zetia
Package Description 7 TABLET in 1 BLISTER PACK (66582-414-15)
Product NDC 66582-414
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ezetimibe
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20021025
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme 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