HYLENEX Recombinant (Baxter Healthcare Corporation)


Welcome to the PulseAid listing for the HYLENEX Recombinant drug offered from Baxter Healthcare Corporation. This Endoglycosidase [EPC],Glycoside Hydrolases [Chemical/Ingredient] 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: Baxter Healthcare Corporation
NON-PROPRIETARY NAME: Hyaluronidase Recombinant Human
SUBSTANCE NAME: HYALURONIDASE RECOMBINANT HUMAN
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Endoglycosidase [EPC],Glycoside Hydrolases [Chemical/Ingredient]
ROUTE: SUBCUTANEOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2005-12-02
END MARKETING DATE: 0000-00-00


HYLENEX Recombinant HUMAN PRESCRIPTION DRUG Details:

Item DescriptionHYLENEX Recombinant from Baxter Healthcare Corporation
LABELER NAME: Baxter Healthcare Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 150([USP’U]/mL)
START MARKETING DATE: 2005-12-02
END MARKETING DATE: 0000-00-00
PRODUCT ID: 60977-319_07eb92e1-3c44-4567-bbec-a24ed0b39c8a
PRODUCT NDC: 60977-319
APPLICATION NUMBER: NDA021859

Other HYALURONIDASE RECOMBINANT HUMAN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Baxter Healthcare CorporationHYLENEX Recombinant