Fludarabine phosphate (Actavis Pharma, Inc.)
Welcome to the PulseAid listing for the Fludarabine phosphate drug offered from Actavis Pharma, Inc.. This Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] 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: | Actavis Pharma, Inc. |
NON-PROPRIETARY NAME: | Fludarabine phosphate |
SUBSTANCE NAME: | FLUDARABINE PHOSPHATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2015-01-05 |
END MARKETING DATE: | 0000-00-00 |
Fludarabine phosphate HUMAN PRESCRIPTION DRUG Details:
Item Description | Fludarabine phosphate from Actavis Pharma, Inc. |
LABELER NAME: | Actavis Pharma, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 50(mg/2mL) |
START MARKETING DATE: | 2015-01-05 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 45963-609_75709606-99c0-48c4-9674-7342de1815c6 |
PRODUCT NDC: | 45963-609 |
APPLICATION NUMBER: | ANDA078610 |
Other FLUDARABINE PHOSPHATE Pharmaceutical Manufacturers / Labelers: