CYTARABINE (Hospira, Inc.)
Welcome to the PulseAid listing for the CYTARABINE drug offered from Hospira, 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: | Hospira, Inc. |
NON-PROPRIETARY NAME: | CYTARABINE |
SUBSTANCE NAME: | CYTARABINE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 1990-08-31 |
END MARKETING DATE: | 0000-00-00 |
CYTARABINE HUMAN PRESCRIPTION DRUG Details:
Item Description | CYTARABINE from Hospira, Inc. |
LABELER NAME: | Hospira, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 20(mg/mL) |
START MARKETING DATE: | 1990-08-31 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 61703-303_ec59aad2-fa83-46ec-acbf-e85ba890c3f5 |
PRODUCT NDC: | 61703-303 |
APPLICATION NUMBER: | ANDA072168 |
Other CYTARABINE Pharmaceutical Manufacturers / Labelers: