Viread (REMEDYREPACK INC.)


Welcome to the PulseAid listing for the Viread drug offered from REMEDYREPACK INC.. This Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Hepatitis B 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: REMEDYREPACK INC.
NON-PROPRIETARY NAME: TENOFOVIR DISOPROXIL FUMARATE
SUBSTANCE NAME: TENOFOVIR DISOPROXIL FUMARATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2017-05-18
END MARKETING DATE: 0000-00-00


Viread HUMAN PRESCRIPTION DRUG Details:

Item DescriptionViread from REMEDYREPACK INC.
LABELER NAME: REMEDYREPACK INC.
DEA SCHEDULE:
ACTIVE STRENGTH: 300(mg/1)
START MARKETING DATE: 2017-05-18
END MARKETING DATE: 0000-00-00
PRODUCT ID: 70518-0546_4fd455b2-031b-049f-e054-00144ff8d46c
PRODUCT NDC: 70518-0546
APPLICATION NUMBER: NDA021356

Other TENOFOVIR DISOPROXIL FUMARATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
A-S Medication SolutionsViread
Avera McKennan HospitalViread
Gilead Sciences, Inc.Viread
REMEDYREPACK INC.Viread
State of Florida DOH Central PharmacyViread