fomepizole (Sandoz Inc.)


Welcome to the PulseAid listing for the fomepizole drug offered from Sandoz Inc.. This Antidote [EPC] 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: Sandoz Inc.
NON-PROPRIETARY NAME: fomepizole
SUBSTANCE NAME: FOMEPIZOLE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Antidote [EPC]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2008-03-06
END MARKETING DATE: 0000-00-00


fomepizole HUMAN PRESCRIPTION DRUG Details:

Item Descriptionfomepizole from Sandoz Inc.
LABELER NAME: Sandoz Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1(g/mL)
START MARKETING DATE: 2008-03-06
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0781-3182_a306cd11-9acf-45f1-91ec-9fef2b08fdb1
PRODUCT NDC: 0781-3182
APPLICATION NUMBER: ANDA078537

Other FOMEPIZOLE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Mylan Institutional LLCFomepizole
PALADIN LABORATORIES (USA) INCAntizol
Sandoz Inc.fomepizole
X-GEN Pharmaceuticalsfomepizole