clofarabine (sanofi-aventis U.S. LLC)


Welcome to the PulseAid listing for the clofarabine drug offered from sanofi-aventis U.S. 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: sanofi-aventis U.S. LLC
NON-PROPRIETARY NAME: clofarabine
SUBSTANCE NAME: CLOFARABINE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION
MARKETING CATEGORY NAME: NDA AUTHORIZED GENERIC
START MARKETING DATE: 2017-05-11
END MARKETING DATE: 0000-00-00


clofarabine HUMAN PRESCRIPTION DRUG Details:

Item Descriptionclofarabine from sanofi-aventis U.S. LLC
LABELER NAME: sanofi-aventis U.S. LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 1(mg/mL)
START MARKETING DATE: 2017-05-11
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0955-1746_d5edb873-461d-47ce-8337-ce24d6151828
PRODUCT NDC: 0955-1746
APPLICATION NUMBER: NDA021673

Other CLOFARABINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Amneal Biosciences LLCClofarabine
Fresenius-KabiCLOFARABINE
Mylan Institutional LLCclofarabine
sanofi-aventis U.S. LLCClolar