Package 84549-072-10

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84549-072-10
Digits Only 8454907210
Product NDC 84549-072
Product ID 84549-072_3f2bb95a-aece-c0b7-e063-6394a90a627b
Description

10 mL in 1 VIAL, GLASS (84549-072-10)

Marketing

Marketing Status
Marketed Since 2025-09-19
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": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "3f2bb95a-aece-c0b7-e063-6394a90a627b", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191222"], "spl_set_id": ["3f2bb95a-aeca-c0b7-e063-6394a90a627b"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, GLASS (84549-072-10)", "package_ndc": "84549-072-10", "marketing_start_date": "20250919"}], "brand_name": "Naloxone Hydrochloride", "product_id": "84549-072_3f2bb95a-aece-c0b7-e063-6394a90a627b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "84549-072", "generic_name": "Naloxone Hydrochloride", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA207634", "marketing_category": "ANDA", "marketing_start_date": "20170726", "listing_expiration_date": "20261231"}