Package 0409-1215-01

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0409-1215-01
Digits Only 0409121501
Product NDC 0409-1215
Product ID 0409-1215_2b456953-1487-4550-946e-50c01536c8ad
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1215-01) / 1 mL in 1 VIAL, SINGLE-DOSE (0409-1215-21)

Marketing

Marketing Status
Marketed Since 2005-07-12
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": "2b456953-1487-4550-946e-50c01536c8ad", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191222", "1659929"], "spl_set_id": ["8535cc84-ad4a-4d67-8480-fb5a2e3406f8"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1215-01)  / 1 mL in 1 VIAL, SINGLE-DOSE (0409-1215-21)", "package_ndc": "0409-1215-01", "marketing_start_date": "20050712"}], "brand_name": "Naloxone Hydrochloride", "product_id": "0409-1215_2b456953-1487-4550-946e-50c01536c8ad", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0409-1215", "generic_name": "NALOXONE HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA070256", "marketing_category": "ANDA", "marketing_start_date": "20050712", "listing_expiration_date": "20261231"}