Package 67457-987-10

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67457-987-10
Digits Only 6745798710
Product NDC 67457-987
Product ID 67457-987_4f711224-09e7-4c4e-8780-e7e76c572f8c
Description

10 VIAL, MULTI-DOSE in 1 CARTON (67457-987-10) / 10 mL in 1 VIAL, MULTI-DOSE (67457-987-00)

Marketing

Marketing Status
Marketed Since 2019-11-20
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": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "4f711224-09e7-4c4e-8780-e7e76c572f8c", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191222"], "spl_set_id": ["8eb8cb6a-8e50-4f22-a516-6831552baa0d"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (67457-987-10)  / 10 mL in 1 VIAL, MULTI-DOSE (67457-987-00)", "package_ndc": "67457-987-10", "marketing_start_date": "20191120"}], "brand_name": "Naloxone Hydrochloride", "product_id": "67457-987_4f711224-09e7-4c4e-8780-e7e76c572f8c", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "67457-987", "generic_name": "naloxone hydrochloride", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA205014", "marketing_category": "ANDA", "marketing_start_date": "20191120", "listing_expiration_date": "20261231"}