Viramune (Boehringer Ingelheim Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Viramune drug offered from Boehringer Ingelheim Pharmaceuticals Inc.. This Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | Boehringer Ingelheim Pharmaceuticals Inc. |
NON-PROPRIETARY NAME: | nevirapine |
SUBSTANCE NAME: | NEVIRAPINE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2001-08-01 |
END MARKETING DATE: | 0000-00-00 |
Viramune HUMAN PRESCRIPTION DRUG Details:
Item Description | Viramune from Boehringer Ingelheim Pharmaceuticals Inc. |
LABELER NAME: | Boehringer Ingelheim Pharmaceuticals Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 200(mg/1) |
START MARKETING DATE: | 2001-08-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0597-0046_554913e8-f01f-4bdb-ccb0-772852a7424b |
PRODUCT NDC: | 0597-0046 |
APPLICATION NUMBER: | NDA020636 |
Other NEVIRAPINE Pharmaceutical Manufacturers / Labelers: