Package 71872-7009-1

Brand: naloxone hydrochloride

Generic: nalxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71872-7009-1
Digits Only 7187270091
Product NDC 71872-7009
Product ID 71872-7009_fa45551b-cd87-d4cc-e053-6294a90a8829
Description

1 VIAL in 1 BAG (71872-7009-1) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2019-05-06
Brand naloxone hydrochloride
Generic nalxone 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": "fa45551b-cd87-d4cc-e053-6294a90a8829", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["8959171f-eda6-158c-e053-2995a90a36b2"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (71872-7009-1)  / 1 mL in 1 VIAL", "package_ndc": "71872-7009-1", "marketing_start_date": "20190506"}], "brand_name": "Naloxone Hydrochloride", "product_id": "71872-7009_fa45551b-cd87-d4cc-e053-6294a90a8829", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71872-7009", "generic_name": "Nalxone 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": "ANDA070299", "marketing_category": "ANDA", "marketing_start_date": "19860924", "listing_expiration_date": "20261231"}