NEVIRAPINE (Cipla USA Inc.)
Welcome to the PulseAid listing for the NEVIRAPINE drug offered from Cipla USA 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: | Cipla USA 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, EXTENDED RELEASE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2015-10-15 |
END MARKETING DATE: | 0000-00-00 |
NEVIRAPINE HUMAN PRESCRIPTION DRUG Details:
Item Description | NEVIRAPINE from Cipla USA Inc. |
LABELER NAME: | Cipla USA Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 400(mg/1) |
START MARKETING DATE: | 2015-10-15 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 69097-403_1c8001da-21e7-4f41-a38f-9c4ee04ecd30 |
PRODUCT NDC: | 69097-403 |
APPLICATION NUMBER: | ANDA206448 |
Other NEVIRAPINE Pharmaceutical Manufacturers / Labelers: