Package 71872-7177-1

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71872-7177-1
Digits Only 7187271771
Product NDC 71872-7177
Product ID 71872-7177_fbbce2ae-1daa-b037-e053-6394a90a3397
Description

1 SYRINGE in 1 BAG (71872-7177-1) / 2 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2019-09-09
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": ["PARENTERAL"], "spl_id": "fbbce2ae-1daa-b037-e053-6394a90a3397", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191250"], "spl_set_id": ["958577c3-d2c4-26ad-e053-2a95a90ad73a"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 BAG (71872-7177-1)  / 2 mL in 1 SYRINGE", "package_ndc": "71872-7177-1", "marketing_start_date": "20190909"}], "brand_name": "Naloxone Hydrochloride", "product_id": "71872-7177_fbbce2ae-1daa-b037-e053-6394a90a3397", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71872-7177", "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": "ANDA072076", "marketing_category": "ANDA", "marketing_start_date": "20010601", "listing_expiration_date": "20261231"}