Package 0517-0710-88

Brand: fomepizole

Generic: fomepizole
NDC Package

Package Facts

Identity

Package NDC 0517-0710-88
Digits Only 0517071088
Product NDC 0517-0710
Description

1 VIAL in 1 CARTON (0517-0710-88) / 1.5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2020-07-31
Brand fomepizole
Generic fomepizole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "aac796de-58f6-49e5-b959-f95b0c7b8889", "openfda": {"nui": ["N0000175429"], "unii": ["83LCM6L2BY"], "rxcui": ["310414"], "spl_set_id": ["a31d0148-2729-49de-b666-f24b0dfd2401"], "pharm_class_epc": ["Antidote [EPC]"], "manufacturer_name": ["American Regent, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0517-0710-88)  / 1.5 mL in 1 VIAL", "package_ndc": "0517-0710-88", "marketing_start_date": "20200731"}], "brand_name": "fomepizole", "product_id": "0517-0710_aac796de-58f6-49e5-b959-f95b0c7b8889", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antidote [EPC]"], "product_ndc": "0517-0710", "generic_name": "fomepizole", "labeler_name": "American Regent, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "fomepizole", "active_ingredients": [{"name": "FOMEPIZOLE", "strength": "1 g/mL"}], "application_number": "ANDA078368", "marketing_category": "ANDA", "marketing_start_date": "20200731", "listing_expiration_date": "20261231"}