Portrazza (Eli Lilly and Company)


Welcome to the PulseAid listing for the Portrazza drug offered from Eli Lilly and Company. This Epidermal Growth Factor Receptor Antagonist [EPC],HER1 Antagonists [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: Eli Lilly and Company
NON-PROPRIETARY NAME: necitumumab
SUBSTANCE NAME: NECITUMUMAB
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Epidermal Growth Factor Receptor Antagonist [EPC],HER1 Antagonists [MoA]
ROUTE: INTRAVENOUS
DOSAGE FORM: SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2015-11-24
END MARKETING DATE: 0000-00-00


Portrazza HUMAN PRESCRIPTION DRUG Details:

Item DescriptionPortrazza from Eli Lilly and Company
LABELER NAME: Eli Lilly and Company
DEA SCHEDULE:
ACTIVE STRENGTH: 16(mg/mL)
START MARKETING DATE: 2015-11-24
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0002-7716_62de9272-71de-4b81-8ccf-ad7806f02081
PRODUCT NDC: 0002-7716
APPLICATION NUMBER: BLA125547

Other NECITUMUMAB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Eli Lilly and CompanyPortrazza