Zetia - 49999-487-90 - (Ezetimibe)

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Drug Information of Zetia

Product NDC: 49999-487
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: 49999-487
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021445
Marketing Category: NDA
Start Marketing Date: 20120319

Package Information of Zetia

Package NDC: 49999-487-90
Package Description: 90 TABLET in 1 BOTTLE (49999-487-90)

NDC Information of Zetia

NDC Code 49999-487-90
Proprietary Name Zetia
Package Description 90 TABLET in 1 BOTTLE (49999-487-90)
Product NDC 49999-487
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ezetimibe
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120319
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products 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