Package 45802-578-84

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 45802-578-84
Digits Only 4580257884
Product NDC 45802-578
Product ID 45802-578_10534467-f259-44bb-bdf7-b09de54411ed
Description

2 VIAL, SINGLE-DOSE in 1 CARTON (45802-578-84) / .1 mL in 1 VIAL, SINGLE-DOSE (45802-578-00)

Marketing

Marketing Status
Marketed Since 2023-07-30
Brand naloxone hydrochloride
Generic naloxone hydrochloride
Sample Package No

Linked Drug Pages (1)

NALOXONE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "10534467-f259-44bb-bdf7-b09de54411ed", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["b5d40220-f194-4835-b70c-f304ecb222d5"], "manufacturer_name": ["Padagis Israel Pharmaceuticals Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 VIAL, SINGLE-DOSE in 1 CARTON (45802-578-24)  / .1 mL in 1 VIAL, SINGLE-DOSE (45802-578-00)", "package_ndc": "45802-578-24", "marketing_start_date": "20250801"}, {"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (45802-578-84)  / .1 mL in 1 VIAL, SINGLE-DOSE (45802-578-00)", "package_ndc": "45802-578-84", "marketing_start_date": "20230730"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "45802-578_10534467-f259-44bb-bdf7-b09de54411ed", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "45802-578", "generic_name": "naloxone hydrochloride", "labeler_name": "Padagis Israel Pharmaceuticals Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NALOXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA211951", "marketing_category": "ANDA", "marketing_start_date": "20230730", "listing_expiration_date": "20271231"}