Mozobil (sanofi-aventis U.S. LLC)


Welcome to the PulseAid listing for the Mozobil drug offered from sanofi-aventis U.S. LLC. This Hematopoietic Stem Cell Mobilizer [EPC],Increased Hematopoietic Stem Cell Mobilization [PE] 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: PLERIXAFOR
SUBSTANCE NAME: PLERIXAFOR
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Hematopoietic Stem Cell Mobilizer [EPC],Increased Hematopoietic Stem Cell Mobilization [PE]
ROUTE: SUBCUTANEOUS
DOSAGE FORM: SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2013-09-01
END MARKETING DATE: 0000-00-00


Mozobil HUMAN PRESCRIPTION DRUG Details:

Item DescriptionMozobil from sanofi-aventis U.S. LLC
LABELER NAME: sanofi-aventis U.S. LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 24(mg/1.2mL)
START MARKETING DATE: 2013-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0024-5862_88f93cdb-26f8-414a-8ad6-96ca0d098ec1
PRODUCT NDC: 0024-5862
APPLICATION NUMBER: NDA022311

Other PLERIXAFOR Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Genzyme CorporationMozobil
sanofi-aventis U.S. LLCMozobil