Package 70069-072-10

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70069-072-10
Digits Only 7006907210
Product NDC 70069-072
Product ID 70069-072_7a544942-0f60-4ed3-91df-049b7f74812e
Description

10 CARTON in 1 BOX (70069-072-10) / 1 VIAL, GLASS in 1 CARTON (70069-072-01) / 10 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2017-07-26
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": "7a544942-0f60-4ed3-91df-049b7f74812e", "openfda": {"upc": ["0370069072011"], "unii": ["F850569PQR"], "rxcui": ["1191222"], "spl_set_id": ["b59ee3cc-9604-4abc-81be-897e2f42aa67"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CARTON in 1 BOX (70069-072-10)  / 1 VIAL, GLASS in 1 CARTON (70069-072-01)  / 10 mL in 1 VIAL, GLASS", "package_ndc": "70069-072-10", "marketing_start_date": "20170726"}], "brand_name": "Naloxone Hydrochloride", "product_id": "70069-072_7a544942-0f60-4ed3-91df-049b7f74812e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "70069-072", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA207634", "marketing_category": "ANDA", "marketing_start_date": "20170726", "listing_expiration_date": "20261231"}