Package 50090-6491-0

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6491-0
Digits Only 5009064910
Product NDC 50090-6491
Product ID 50090-6491_139efb34-7bd4-46a7-9aeb-20e7b973d7a2
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (50090-6491-0) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2023-05-19
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": "139efb34-7bd4-46a7-9aeb-20e7b973d7a2", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["3d2dcee4-7510-477b-95a8-9b2afb773984"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (50090-6491-0)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "50090-6491-0", "marketing_start_date": "20230519"}], "brand_name": "Naloxone Hydrochloride", "product_id": "50090-6491_139efb34-7bd4-46a7-9aeb-20e7b973d7a2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "50090-6491", "generic_name": "naloxone hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA204997", "marketing_category": "ANDA", "marketing_start_date": "20140306", "listing_expiration_date": "20261231"}