Package 71872-7198-1

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71872-7198-1
Digits Only 7187271981
Product NDC 71872-7198
Product ID 71872-7198_fb4adbb5-bf2e-f855-e053-6294a90a8e7b
Description

1 VIAL in 1 BAG (71872-7198-1) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2020-01-29
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": "fb4adbb5-bf2e-f855-e053-6294a90a8e7b", "openfda": {"upc": ["0370069071014"], "unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["9e53f169-4a6e-6102-e053-2995a90ab3dc"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (71872-7198-1)  / 1 mL in 1 VIAL", "package_ndc": "71872-7198-1", "marketing_start_date": "20200129"}], "brand_name": "Naloxone Hydrochloride", "product_id": "71872-7198_fb4adbb5-bf2e-f855-e053-6294a90a8e7b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71872-7198", "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": "ANDA207633", "marketing_category": "ANDA", "marketing_start_date": "20170808", "listing_expiration_date": "20261231"}