LeukoTrap SOLX B Additive (Haemonetics Manufacturing Inc)


Welcome to the PulseAid listing for the LeukoTrap SOLX B Additive drug offered from Haemonetics Manufacturing Inc. 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: Haemonetics Manufacturing Inc
NON-PROPRIETARY NAME: AS-7 B Additive Solution
SUBSTANCE NAME: DEXTROSE, UNSPECIFIED FORM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: INTRAVENOUS
DOSAGE FORM: SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2015-11-12
END MARKETING DATE: 0000-00-00


LeukoTrap SOLX B Additive HUMAN PRESCRIPTION DRUG Details:

Item DescriptionLeukoTrap SOLX B Additive from Haemonetics Manufacturing Inc
LABELER NAME: Haemonetics Manufacturing Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 1.78(g/30mL)
START MARKETING DATE: 2015-11-12
END MARKETING DATE: 0000-00-00
PRODUCT ID: 53157-000_eab5a1f9-bed2-4a42-9544-d5912cd267b8
PRODUCT NDC: 53157-000
APPLICATION NUMBER: NDA110059

Other DEXTROSE, UNSPECIFIED FORM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Haemonetics Manufacturing IncLeukoTrap SOLX B Additive