Gemcitabine (Athenex Pharmaceutical Division, LLC.)
Welcome to the PulseAid listing for the Gemcitabine drug offered from Athenex Pharmaceutical Division, LLC.. 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: | Athenex Pharmaceutical Division, LLC. |
NON-PROPRIETARY NAME: | gemcitabine hydrochloride |
SUBSTANCE NAME: | GEMCITABINE HYDROCHLORIDE |
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: | 2017-07-31 |
END MARKETING DATE: | 0000-00-00 |
Gemcitabine HUMAN PRESCRIPTION DRUG Details:
Item Description | Gemcitabine from Athenex Pharmaceutical Division, LLC. |
LABELER NAME: | Athenex Pharmaceutical Division, LLC. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 200(mg/5mL) |
START MARKETING DATE: | 2017-07-31 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 70860-204_812a8ac5-60d5-4fde-8b3c-8ca241744f1d |
PRODUCT NDC: | 70860-204 |
APPLICATION NUMBER: | ANDA204520 |
Other GEMCITABINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: