ZERIT (State of Florida DOH Central Pharmacy)


Welcome to the PulseAid listing for the ZERIT drug offered from State of Florida DOH Central Pharmacy. 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: State of Florida DOH Central Pharmacy
NON-PROPRIETARY NAME: stavudine
SUBSTANCE NAME: STAVUDINE
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, GELATIN COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2009-07-01
END MARKETING DATE: 0000-00-00


ZERIT HUMAN PRESCRIPTION DRUG Details:

Item DescriptionZERIT from State of Florida DOH Central Pharmacy
LABELER NAME: State of Florida DOH Central Pharmacy
DEA SCHEDULE:
ACTIVE STRENGTH: 40(mg/1)
START MARKETING DATE: 2009-07-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 53808-0795_66893c23-b206-4107-ad2b-1af596b4c5c5
PRODUCT NDC: 53808-0795
APPLICATION NUMBER: NDA020412

Other STAVUDINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Aurobindo Pharma LimitedStavudine
Camber Pharmaceuticals, Inc.Stavudine
Cipla Ltd.stavudine
Citron Pharma LLCStavudine
E.R. Squibb & Sons, L.L.C.ZERIT
KAISER FOUNDATION HOSPITALSStavudine
Mylan Pharmaceuticals Inc.Stavudine
Rising Pharmaceuticals, Inc.Stavudine
State of Florida DOH Central PharmacyZERIT