Renflexis (Merck Sharp & Dohme Corp.)


Welcome to the PulseAid listing for the Renflexis drug offered from Merck Sharp & Dohme Corp.. 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: Merck Sharp & Dohme Corp.
NON-PROPRIETARY NAME: infliximab
SUBSTANCE NAME: INFLIXIMAB
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: 2017-07-01
END MARKETING DATE: 0000-00-00


Renflexis HUMAN PRESCRIPTION DRUG Details:

Item DescriptionRenflexis from Merck Sharp & Dohme Corp.
LABELER NAME: Merck Sharp & Dohme Corp.
DEA SCHEDULE:
ACTIVE STRENGTH: 100(mg/1)
START MARKETING DATE: 2017-07-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0006-4305_80f9dcfe-a91b-405e-ae61-cc2895d43084
PRODUCT NDC: 0006-4305
APPLICATION NUMBER: BLA761054

Other INFLIXIMAB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Merck Sharp & Dohme Corp.Renflexis