Actemra (Genentech, Inc.)


Welcome to the PulseAid listing for the Actemra drug offered from Genentech, Inc.. This Interleukin 6 Receptor Antagonists [MoA],Interleukin-6 Receptor Antagonist [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: tocilizumab
SUBSTANCE NAME: TOCILIZUMAB
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Interleukin 6 Receptor Antagonists [MoA],Interleukin-6 Receptor Antagonist [EPC]
ROUTE: SUBCUTANEOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2013-10-21
END MARKETING DATE: 0000-00-00


Actemra HUMAN PRESCRIPTION DRUG Details:

Item DescriptionActemra from Genentech, Inc.
LABELER NAME: Genentech, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 180(mg/mL)
START MARKETING DATE: 2013-10-21
END MARKETING DATE: 0000-00-00
PRODUCT ID: 50242-138_494568f6-cc02-4df4-8a18-7d910156b178
PRODUCT NDC: 50242-138
APPLICATION NUMBER: BLA125472

Other TOCILIZUMAB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Genentech, Inc.ACTEMRA