VITRASE (Bausch & Lomb Incorporated)


Welcome to the PulseAid listing for the VITRASE drug offered from Bausch & Lomb Incorporated. 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: Bausch & Lomb Incorporated
NON-PROPRIETARY NAME: hyaluronidase, ovine
SUBSTANCE NAME: HYALURONIDASE, OVINE
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: 2005-02-01
END MARKETING DATE: 0000-00-00


VITRASE HUMAN PRESCRIPTION DRUG Details:

Item DescriptionVITRASE from Bausch & Lomb Incorporated
LABELER NAME: Bausch & Lomb Incorporated
DEA SCHEDULE:
ACTIVE STRENGTH: 200([USP’U]/mL)
START MARKETING DATE: 2005-02-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 24208-002_230ed4da-acbf-4cf5-9626-bff59c221007
PRODUCT NDC: 24208-002
APPLICATION NUMBER: NDA021640

Other HYALURONIDASE, OVINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Bausch & Lomb IncorporatedVITRASE
ISTA Pharmaceuticals, Inc.VITRASE