Package 50090-2422-0

Brand: narcan

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-2422-0
Digits Only 5009024220
Product NDC 50090-2422
Description

2 VIAL, SINGLE-DOSE in 1 PACKAGE (50090-2422-0) / .1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2017-01-24
Brand narcan
Generic naloxone hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "caf3eabb-89bd-469a-9d00-3fd3a18fb5db", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059", "1725064"], "spl_set_id": ["139c30b9-5600-48f5-8610-0cacd2782398"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 PACKAGE (50090-2422-0)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "50090-2422-0", "marketing_start_date": "20170124"}], "brand_name": "NARCAN", "product_id": "50090-2422_caf3eabb-89bd-469a-9d00-3fd3a18fb5db", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "50090-2422", "generic_name": "Naloxone Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NARCAN", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "NDA208411", "marketing_category": "NDA", "marketing_start_date": "20170124", "listing_expiration_date": "20261231"}