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Intelence
Intelence - 24236-679-21 - (etravirine)
Drug Information of Intelence
| Product NDC: | 24236-679 |
| 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: | 24236-679 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022187 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130318 |
Package Information of Intelence
| Package NDC: | 24236-679-21 |
| Package Description: | 120 TABLET in 1 CANISTER (24236-679-21) |
NDC Information of Intelence
| NDC Code | 24236-679-21 |
| Proprietary Name | Intelence |
| Package Description | 120 TABLET in 1 CANISTER (24236-679-21) |
| Product NDC | 24236-679 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | etravirine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130318 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| 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] |
