Package 71872-7215-1

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71872-7215-1
Digits Only 7187272151
Product NDC 71872-7215
Product ID 71872-7215_facf199d-f6dd-926f-e053-6294a90ad1ee
Description

1 VIAL, MULTI-DOSE in 1 BAG (71872-7215-1) / 10 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2020-06-15
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": "facf199d-f6dd-926f-e053-6294a90ad1ee", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191222"], "spl_set_id": ["ada6856c-5293-fc2f-e053-2995a90a8ec6"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 BAG (71872-7215-1)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71872-7215-1", "marketing_start_date": "20200615"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "71872-7215_facf199d-f6dd-926f-e053-6294a90ad1ee", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71872-7215", "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": "ANDA212456", "marketing_category": "ANDA", "marketing_start_date": "20191104", "listing_expiration_date": "20261231"}