Emtriva (Excella GmbH)


Welcome to the PulseAid listing for the Emtriva drug offered from Excella GmbH. 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: Excella GmbH
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: CAPSULE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2003-07-02
END MARKETING DATE: 0000-00-00


Emtriva HUMAN PRESCRIPTION DRUG Details:

Item DescriptionEmtriva from Excella GmbH
LABELER NAME: Excella GmbH
DEA SCHEDULE:
ACTIVE STRENGTH: 200(mg/1)
START MARKETING DATE: 2003-07-02
END MARKETING DATE: 0000-00-00
PRODUCT ID: 46014-0601_1920b87b-ac14-4b51-ae82-9ccf51f1b00e
PRODUCT NDC: 46014-0601
APPLICATION NUMBER: NDA021500

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