Package 71872-7326-1

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71872-7326-1
Digits Only 7187273261
Product NDC 71872-7326
Description

1 CARTON in 1 BAG (71872-7326-1) / 1 VIAL, GLASS in 1 CARTON / 10 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2024-06-19
Brand naloxone hydrochloride
Generic naloxone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "28f3d32d-b65b-5c4c-e063-6394a90ae561", "openfda": {"upc": ["0370069072011"], "unii": ["F850569PQR"], "rxcui": ["1191222"], "spl_set_id": ["28f3e3bc-b1be-9f06-e063-6394a90a1936"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 CARTON in 1 BAG (71872-7326-1)  / 1 VIAL, GLASS in 1 CARTON / 10 mL in 1 VIAL, GLASS", "package_ndc": "71872-7326-1", "marketing_start_date": "20240619"}], "brand_name": "Naloxone Hydrochloride", "product_id": "71872-7326_28f3d32d-b65b-5c4c-e063-6394a90ae561", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71872-7326", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Medical Purchasing Solutions, LLC", "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"}