Package 59467-679-01

Brand: kloxxado

Generic: naloxone hcl
NDC Package

Package Facts

Identity

Package NDC 59467-679-01
Digits Only 5946767901
Product NDC 59467-679
Product ID 59467-679_da424329-9a63-4df3-bced-4157d2086e20
Description

.1 mL in 1 VIAL, SINGLE-DOSE (59467-679-01)

Marketing

Marketing Status
Marketed Since 2021-08-03
Brand kloxxado
Generic naloxone hcl
Sample Package No

Linked Drug Pages (1)

KLOXXADO ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "da424329-9a63-4df3-bced-4157d2086e20", "openfda": {"upc": ["0359467679015"], "unii": ["F850569PQR"], "rxcui": ["2540703", "2540709"], "spl_set_id": ["ebf0f833-c1c0-487c-8f29-01fa8c61b6cb"], "manufacturer_name": ["Hikma Specialty USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".1 mL in 1 VIAL, SINGLE-DOSE (59467-679-01)", "package_ndc": "59467-679-01", "marketing_start_date": "20210803"}], "brand_name": "KLOXXADO", "product_id": "59467-679_da424329-9a63-4df3-bced-4157d2086e20", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "59467-679", "generic_name": "Naloxone HCL", "labeler_name": "Hikma Specialty USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KLOXXADO", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "8 mg/.1mL"}], "application_number": "NDA212045", "marketing_category": "NDA", "marketing_start_date": "20210803", "listing_expiration_date": "20261231"}