ZINPLAVA (Merck Sharp & Dohme Corp.)


Welcome to the PulseAid listing for the ZINPLAVA drug offered from Merck Sharp & Dohme Corp.. This 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: bezlotoxumab
SUBSTANCE NAME: BEZLOTOXUMAB
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2016-10-21
END MARKETING DATE: 0000-00-00


ZINPLAVA HUMAN PRESCRIPTION DRUG Details:

Item DescriptionZINPLAVA from Merck Sharp & Dohme Corp.
LABELER NAME: Merck Sharp & Dohme Corp.
DEA SCHEDULE:
ACTIVE STRENGTH: 25(mg/mL)
START MARKETING DATE: 2016-10-21
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0006-3025_d6c5254f-8153-4861-b4ad-6f439fed4b63
PRODUCT NDC: 0006-3025
APPLICATION NUMBER: BLA761046

Other BEZLOTOXUMAB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Merck Sharp & Dohme Corp.ZINPLAVA