Emtriva (Gilead Sciences, Inc.)


Welcome to the PulseAid listing for the Emtriva drug offered from Gilead Sciences, Inc.. This Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase 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: Gilead Sciences, Inc.
NON-PROPRIETARY NAME: EMTRICITABINE
SUBSTANCE NAME: EMTRICITABINE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2005-09-28
END MARKETING DATE: 0000-00-00


Emtriva HUMAN PRESCRIPTION DRUG Details:

Item DescriptionEmtriva from Gilead Sciences, Inc.
LABELER NAME: Gilead Sciences, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 10(mg/mL)
START MARKETING DATE: 2005-09-28
END MARKETING DATE: 0000-00-00
PRODUCT ID: 61958-0602_9d004165-8e41-4b34-97e5-fca88062969c
PRODUCT NDC: 61958-0602
APPLICATION NUMBER: NDA021896

Other EMTRICITABINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Excella GmbHEmtriva
Gilead Sciences, Inc.Emtriva
Physicians Total Care, Inc.Emtriva
State of Florida DOH Central PharmacyEmtriva