LUCENTIS (Genentech, Inc.)


Welcome to the PulseAid listing for the LUCENTIS drug offered from Genentech, Inc.. This Vascular Endothelial Growth Factor Inhibitors [MoA],Vascular Endothelial Growth Factor Inhibitor [EPC] 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: Genentech, Inc.
NON-PROPRIETARY NAME: RANIBIZUMAB
SUBSTANCE NAME: RANIBIZUMAB
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Vascular Endothelial Growth Factor Inhibitors [MoA],Vascular Endothelial Growth Factor Inhibitor [EPC]
ROUTE: INTRAVITREAL
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2006-06-30
END MARKETING DATE: 0000-00-00


LUCENTIS HUMAN PRESCRIPTION DRUG Details:

Item DescriptionLUCENTIS from Genentech, Inc.
LABELER NAME: Genentech, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 10(mg/mL)
START MARKETING DATE: 2006-06-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 50242-080_3324ea2f-1ca4-403c-8049-61108762e7c7
PRODUCT NDC: 50242-080
APPLICATION NUMBER: BLA125156

Other RANIBIZUMAB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Genentech, Inc.LUCENTIS