Intelence - 59676-571-01 - (etravirine)

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Drug Information of Intelence

Product NDC: 59676-571
Proprietary Name: Intelence
Non Proprietary Name: etravirine
Active Ingredient(s): 200    mg/1 & nbsp;   etravirine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Intelence

Product NDC: 59676-571
Labeler Name: Janssen Products LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022187
Marketing Category: NDA
Start Marketing Date: 20101222

Package Information of Intelence

Package NDC: 59676-571-01
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (59676-571-01)

NDC Information of Intelence

NDC Code 59676-571-01
Proprietary Name Intelence
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (59676-571-01)
Product NDC 59676-571
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name etravirine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101222
Marketing Category Name NDA
Labeler Name Janssen Products LP
Substance Name ETRAVIRINE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]

Complete Information of Intelence


General Information