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FDA Approval

CRIXIVAN

CompanyState of Florida DOH Central Pharmacy (DUNS: 829348114)

Effective Date

August 18, 2010

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Indinavir(400 mg in 1 1)

Manufacturing Establishments (1)

State of Florida DOH Central Pharmacy

Labeler

State of Florida DOH Central Pharmacy

DUNS Number

829348114

Products (1)

CRIXIVAN

NDC Product Code

53808-0661

Application Number

NDA020685

Marketing Category

NDA (C73594)

Route of Administration

ORAL

Effective Date

August 18, 2010

Ingredients

SODIUM LAURYL SULFATEInactive

Code: 368GB5141JClass: IACT

IndinavirActive

Code: 771H53976QClass: ACTIMQuantity: 400 mg in 1 1

ANHYDROUS LACTOSEInactive

Code: 3SY5LH9PMKClass: IACT

MAGNESIUM STEARATEInactive

Code: 70097M6I30Class: IACT

GELATINInactive

Code: 2G86QN327LClass: IACT

TITANIUM DIOXIDEInactive

Code: 15FIX9V2JPClass: IACT

SILICON DIOXIDEInactive

Code: ETJ7Z6XBU4Class: IACT

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