fomepizole

Generic: fomepizole

Labeler: zydus pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fomepizole
Generic Name fomepizole
Labeler zydus pharmaceuticals usa inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

fomepizole 1 g/mL

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 70710-1478
Product ID 70710-1478_62ff03a3-fb25-41d8-9c6c-d1ad61ea3d31
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078537
Listing Expiration 2026-12-31
Marketing Start 2021-03-18

Pharmacologic Class

Established (EPC)
antidote [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707101478
Hyphenated Format 70710-1478

Supplemental Identifiers

RxCUI
310414
UPC
0370710147815
UNII
83LCM6L2BY
NUI
N0000175429

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name fomepizole (source: ndc)
Generic Name fomepizole (source: ndc)
Application Number ANDA078537 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (70710-1478-1) / 1.5 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

fomepizole (1 g/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "62ff03a3-fb25-41d8-9c6c-d1ad61ea3d31", "openfda": {"nui": ["N0000175429"], "upc": ["0370710147815"], "unii": ["83LCM6L2BY"], "rxcui": ["310414"], "spl_set_id": ["256910fe-91f2-48f6-b0b4-55edc52dacd4"], "pharm_class_epc": ["Antidote [EPC]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (70710-1478-1)  / 1.5 mL in 1 VIAL", "package_ndc": "70710-1478-1", "marketing_start_date": "20210318"}], "brand_name": "Fomepizole", "product_id": "70710-1478_62ff03a3-fb25-41d8-9c6c-d1ad61ea3d31", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antidote [EPC]"], "product_ndc": "70710-1478", "generic_name": "Fomepizole", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fomepizole", "active_ingredients": [{"name": "FOMEPIZOLE", "strength": "1 g/mL"}], "application_number": "ANDA078537", "marketing_category": "ANDA", "marketing_start_date": "20210318", "listing_expiration_date": "20261231"}