Package 0404-9920-01

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9920-01
Digits Only 0404992001
Product NDC 0404-9920
Product ID 0404-9920_60d937e9-a110-40d3-983d-f445518702a9
Description

1 BOX in 1 BAG (0404-9920-01) / 1 CARTRIDGE in 1 BOX / 1 mL in 1 CARTRIDGE

Marketing

Marketing Status
Marketed Since 2022-01-13
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": "60d937e9-a110-40d3-983d-f445518702a9", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191234"], "spl_set_id": ["d39635a4-ddb3-4d32-8211-eb84c78e9f59"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOX in 1 BAG (0404-9920-01)  / 1 CARTRIDGE in 1 BOX / 1 mL in 1 CARTRIDGE", "package_ndc": "0404-9920-01", "marketing_start_date": "20220113"}], "brand_name": "Naloxone Hydrochloride", "product_id": "0404-9920_60d937e9-a110-40d3-983d-f445518702a9", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0404-9920", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Henry Schein, 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": "20220113", "listing_expiration_date": "20261231"}