Package 50090-6963-0

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6963-0
Digits Only 5009069630
Product NDC 50090-6963
Product ID 50090-6963_7a0088db-1e25-49db-9a22-c99cd6adfd8f
Description

2 VIAL, SINGLE-DOSE in 1 CARTON (50090-6963-0) / .1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2023-12-20
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": ["NASAL"], "spl_id": "7a0088db-1e25-49db-9a22-c99cd6adfd8f", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["46f27d04-d4d2-4ef1-9cc5-4d58f4056f06"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (50090-6963-0)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "50090-6963-0", "marketing_start_date": "20231220"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "50090-6963_7a0088db-1e25-49db-9a22-c99cd6adfd8f", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "50090-6963", "generic_name": "naloxone hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NALOXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA211951", "marketing_category": "ANDA", "marketing_start_date": "20230730", "listing_expiration_date": "20261231"}