Zidovudine (DOH CENTRAL PHARMACY)
Welcome to the PulseAid listing for the Zidovudine drug offered from 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: | DOH CENTRAL PHARMACY |
NON-PROPRIETARY NAME: | ZIDOVUDINE |
SUBSTANCE NAME: | ZIDOVUDINE |
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: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2009-07-01 |
END MARKETING DATE: | 0000-00-00 |
Zidovudine HUMAN PRESCRIPTION DRUG Details:
Item Description | Zidovudine from DOH CENTRAL PHARMACY |
LABELER NAME: | DOH CENTRAL PHARMACY |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 300(mg/1) |
START MARKETING DATE: | 2009-07-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 53808-0812_5ecb9e06-5d39-4c3f-87dd-0e8722232880 |
PRODUCT NDC: | 53808-0812 |
APPLICATION NUMBER: | ANDA077267 |
Other ZIDOVUDINE Pharmaceutical Manufacturers / Labelers: