Package 71872-7299-1

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71872-7299-1
Digits Only 7187272991
Product NDC 71872-7299
Product ID 71872-7299_fa1a4689-9121-afd1-e053-6294a90a44ca
Description

1 SYRINGE in 1 BAG (71872-7299-1) / 2 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2023-01-25
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": "fa1a4689-9121-afd1-e053-6294a90a44ca", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191250"], "spl_set_id": ["f9c5efca-443a-41a0-e053-6294a90a8774"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 BAG (71872-7299-1)  / 2 mL in 1 SYRINGE", "package_ndc": "71872-7299-1", "marketing_start_date": "20230125"}], "brand_name": "Naloxone Hydrochloride", "product_id": "71872-7299_fa1a4689-9121-afd1-e053-6294a90a44ca", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71872-7299", "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": "1 mg/mL"}], "application_number": "ANDA213279", "marketing_category": "ANDA", "marketing_start_date": "20210114", "listing_expiration_date": "20261231"}