Package 50090-5908-0

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride nasal
NDC Package

Package Facts

Identity

Package NDC 50090-5908-0
Digits Only 5009059080
Product NDC 50090-5908
Product ID 50090-5908_fefa320d-95d8-414e-ad54-40c9f6d2c55d
Description

2 VIAL, SINGLE-DOSE in 1 CARTON (50090-5908-0) / .1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-01-19
Brand naloxone hydrochloride
Generic naloxone hydrochloride nasal
Sample Package No

Linked Drug Pages (1)

Naloxone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "fefa320d-95d8-414e-ad54-40c9f6d2c55d", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["4517afa1-4b17-4a15-b91b-65b18bd0558f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (50090-5908-0)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "50090-5908-0", "marketing_start_date": "20220119"}], "brand_name": "Naloxone Hydrochloride", "product_id": "50090-5908_fefa320d-95d8-414e-ad54-40c9f6d2c55d", "dosage_form": "INHALANT", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "50090-5908", "generic_name": "Naloxone Hydrochloride Nasal", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "NDA208411", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20211220", "listing_expiration_date": "20261231"}