Nevirapine (Aurobindo Pharma Limited)


Welcome to the PulseAid listing for the Nevirapine drug offered from Aurobindo Pharma Limited. 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: Aurobindo Pharma Limited
NON-PROPRIETARY NAME: Nevirapine
SUBSTANCE NAME: NEVIRAPINE HEMIHYDRATE
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: SUSPENSION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2012-05-22
END MARKETING DATE: 0000-00-00


Nevirapine HUMAN PRESCRIPTION DRUG Details:

Item DescriptionNevirapine from Aurobindo Pharma Limited
LABELER NAME: Aurobindo Pharma Limited
DEA SCHEDULE:
ACTIVE STRENGTH: 50(mg/5mL)
START MARKETING DATE: 2012-05-22
END MARKETING DATE: 0000-00-00
PRODUCT ID: 65862-057_b91b28f6-aab6-40fe-a507-b5df6110d1a9
PRODUCT NDC: 65862-057
APPLICATION NUMBER: ANDA077702

Other NEVIRAPINE HEMIHYDRATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Aurobindo Pharma LimitedNevirapine