Kynamro (Kastle Therapeutics, LLC)


Welcome to the PulseAid listing for the Kynamro drug offered from Kastle Therapeutics, LLC. 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: Kastle Therapeutics, LLC
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: 2016-05-02
END MARKETING DATE: 0000-00-00


Kynamro HUMAN PRESCRIPTION DRUG Details:

Item DescriptionKynamro from Kastle Therapeutics, LLC
LABELER NAME: Kastle Therapeutics, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 200(mg/mL)
START MARKETING DATE: 2016-05-02
END MARKETING DATE: 0000-00-00
PRODUCT ID: 70688-0502_900bb03a-deb5-4522-8dc1-755994b073b6
PRODUCT NDC: 70688-0502
APPLICATION NUMBER: NDA203568

Other MIPOMERSEN SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Genzyme CorporationKynamro
Kastle Therapeutics, LLCKynamro