Kynamro (Genzyme Corporation)


Welcome to the PulseAid listing for the Kynamro drug offered from Genzyme Corporation. This Apolipoprotein B-100 Synthesis Inhibitor [EPC],Decreased Protein Synthesis [PE],Antisense Oligonucleotide [EPC],Oligonucleotides, Antisense [Chemical/Ingredient] 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: Genzyme Corporation
NON-PROPRIETARY NAME: MIPOMERSEN SODIUM
SUBSTANCE NAME: MIPOMERSEN SODIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Apolipoprotein B-100 Synthesis Inhibitor [EPC],Decreased Protein Synthesis [PE],Antisense Oligonucleotide [EPC],Oligonucleotides, Antisense [Chemical/Ingredient]
ROUTE: SUBCUTANEOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2013-01-29
END MARKETING DATE: 0000-00-00


Kynamro HUMAN PRESCRIPTION DRUG Details:

Item DescriptionKynamro from Genzyme Corporation
LABELER NAME: Genzyme Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 200(mg/mL)
START MARKETING DATE: 2013-01-29
END MARKETING DATE: 0000-00-00
PRODUCT ID: 58468-0191_37da4828-7c56-43a3-9c21-8781d5e7d0d2
PRODUCT NDC: 58468-0191
APPLICATION NUMBER: NDA203568

Other MIPOMERSEN SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Genzyme CorporationKynamro
Kastle Therapeutics, LLCKynamro