Intelence - 53808-0787-1 - (Etravirine)

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Drug Information of Intelence

Product NDC: 53808-0787
Proprietary Name: Intelence
Non Proprietary Name: Etravirine
Active Ingredient(s): 100    mg/1 & nbsp;   Etravirine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Intelence

Product NDC: 53808-0787
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022187
Marketing Category: NDA
Start Marketing Date: 20090701

Package Information of Intelence

Package NDC: 53808-0787-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0787-1)

NDC Information of Intelence

NDC Code 53808-0787-1
Proprietary Name Intelence
Package Description 30 TABLET in 1 BLISTER PACK (53808-0787-1)
Product NDC 53808-0787
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etravirine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name NDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name ETRAVIRINE
Strength Number 100
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