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