MedPath

Antizol

Approved
Approval ID

c045b5a8-b220-4f0a-a831-155b29c19454

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jul 27, 2009

Manufacturers
FDA

PALADIN LABORATORIES (USA) INC

DUNS: 831011775

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

fomepizole

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code46129-200
Application NumberNDA020696
Product Classification
M
Marketing Category
C73594
G
Generic Name
fomepizole
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJuly 27, 2009
FDA Product Classification

INGREDIENTS (1)

FOMEPIZOLEActive
Quantity: 1 g in 1 mL
Code: 83LCM6L2BY
Classification: ACTIB

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