INFLECTRA (Pfizer Laboratories Div Pfizer Inc)


Welcome to the PulseAid listing for the INFLECTRA drug offered from Pfizer Laboratories Div Pfizer Inc. This Tumor Necrosis Factor Blocker [EPC],Tumor Necrosis Factor Receptor Blocking Activity [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: Pfizer Laboratories Div Pfizer Inc
NON-PROPRIETARY NAME: infliximab-dyyb
SUBSTANCE NAME: INFLIXIMAB, LICENSE HOLDER UNSPECIFIED
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Tumor Necrosis Factor Blocker [EPC],Tumor Necrosis Factor Receptor Blocking Activity [MoA]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2016-11-21
END MARKETING DATE: 0000-00-00


INFLECTRA HUMAN PRESCRIPTION DRUG Details:

Item DescriptionINFLECTRA from Pfizer Laboratories Div Pfizer Inc
LABELER NAME: Pfizer Laboratories Div Pfizer Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 100(mg/10mL)
START MARKETING DATE: 2016-11-21
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0069-0809_ba28d344-9400-4361-a0cf-5e2fec19c1fc
PRODUCT NDC: 0069-0809
APPLICATION NUMBER: BLA125544

Other INFLIXIMAB, LICENSE HOLDER UNSPECIFIED Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Janssen Biotech, Inc.REMICADE
Pfizer Laboratories Div Pfizer IncINFLECTRA