XELJANZXR (Pfizer Laboratories Div Pfizer Inc)


Welcome to the PulseAid listing for the XELJANZ drug offered from Pfizer Laboratories Div Pfizer Inc. This Janus Kinase Inhibitor [EPC],Janus Kinase Inhibitors [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: tofacitinib
SUBSTANCE NAME: TOFACITINIB CITRATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Janus Kinase Inhibitor [EPC],Janus Kinase Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED, EXTENDED RELEASE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2016-03-07
END MARKETING DATE: 0000-00-00


XELJANZ XR HUMAN PRESCRIPTION DRUG Details:

Item DescriptionXELJANZ XR from Pfizer Laboratories Div Pfizer Inc
LABELER NAME: Pfizer Laboratories Div Pfizer Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 11(mg/1)
START MARKETING DATE: 2016-03-07
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0069-0501_022fd1b8-4c93-4f7c-9a61-8958386c9483
PRODUCT NDC: 0069-0501
APPLICATION NUMBER: NDA208246

Other TOFACITINIB CITRATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Pfizer Laboratories Div Pfizer IncXELJANZ
U.S. PharmaceuticalsXELJANZ