SUSTIVA (REMEDYREPACK INC.)


Welcome to the PulseAid listing for the SUSTIVA drug offered from REMEDYREPACK 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],Cytochrome P450 2C9 Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [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: REMEDYREPACK INC.
NON-PROPRIETARY NAME: efavirenz
SUBSTANCE NAME: EFAVIRENZ
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],Cytochrome P450 2C9 Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2017-05-05
END MARKETING DATE: 0000-00-00


SUSTIVA HUMAN PRESCRIPTION DRUG Details:

Item DescriptionSUSTIVA from REMEDYREPACK INC.
LABELER NAME: REMEDYREPACK INC.
DEA SCHEDULE:
ACTIVE STRENGTH: 600(mg/1)
START MARKETING DATE: 2017-05-05
END MARKETING DATE: 0000-00-00
PRODUCT ID: 70518-0482_4f0c1ed0-f0f9-1e61-e054-00144ff88e88
PRODUCT NDC: 70518-0482
APPLICATION NUMBER: NDA021360

Other EFAVIRENZ Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Bristol-Myers Squibb Pharma CompanySUSTIVA
Physicians Total Care, Inc.SUSTIVA
REMEDYREPACK INC.SUSTIVA