Nplate (Amgen Inc)


Welcome to the PulseAid listing for the Nplate drug offered from Amgen Inc. This Increased Megakaryocyte Maturation [PE],Increased Platelet Production [PE],Thrombopoietin Receptor Agonist [EPC],Thrombopoietin Receptor Agonists [MoA] 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: Amgen Inc
NON-PROPRIETARY NAME: romiplostim
SUBSTANCE NAME: ROMIPLOSTIM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Increased Megakaryocyte Maturation [PE],Increased Platelet Production [PE],Thrombopoietin Receptor Agonist [EPC],Thrombopoietin Receptor Agonists [MoA]
ROUTE: SUBCUTANEOUS
DOSAGE FORM: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2008-08-25
END MARKETING DATE: 0000-00-00


Nplate HUMAN PRESCRIPTION DRUG Details:

Item DescriptionNplate from Amgen Inc
LABELER NAME: Amgen Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 250(ug/.5mL)
START MARKETING DATE: 2008-08-25
END MARKETING DATE: 0000-00-00
PRODUCT ID: 55513-221_af3cf0ec-5402-4893-8ab3-811973c94e47
PRODUCT NDC: 55513-221
APPLICATION NUMBER: BLA125268

Other ROMIPLOSTIM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Amgen IncNplate