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