Package 0409-1782-69

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0409-1782-69
Digits Only 0409178269
Product NDC 0409-1782
Product ID 0409-1782_568bacb5-8e96-46d9-8717-23951594a9fb
Description

10 CARTRIDGE in 1 BOX (0409-1782-69) / 1 mL in 1 CARTRIDGE (0409-1782-03)

Marketing

Marketing Status
Marketed Since 2005-09-23
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": "568bacb5-8e96-46d9-8717-23951594a9fb", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191234"], "spl_set_id": ["b598c237-032d-4bb5-0e92-50eabd863dac"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CARTRIDGE in 1 BOX (0409-1782-69)  / 1 mL in 1 CARTRIDGE (0409-1782-03)", "package_ndc": "0409-1782-69", "marketing_start_date": "20050923"}], "brand_name": "Naloxone Hydrochloride", "product_id": "0409-1782_568bacb5-8e96-46d9-8717-23951594a9fb", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0409-1782", "generic_name": "NALOXONE HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA070172", "marketing_category": "ANDA", "marketing_start_date": "20050923", "listing_expiration_date": "20261231"}