Package 59011-960-10

Brand: nalmefene hydrochloride

Generic: nalmefene hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59011-960-10
Digits Only 5901196010
Product NDC 59011-960
Description

10 VIAL, GLASS in 1 CARTON (59011-960-10) / 2 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2022-02-08
Brand nalmefene hydrochloride
Generic nalmefene hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "ec96ac7c-4d1f-4973-b7de-a7955acbd557", "openfda": {"unii": ["K7K69QC05X"], "rxcui": ["2592953"], "spl_set_id": ["3abfbffc-9e52-4fc6-ae92-6e0a97f4afe7"], "manufacturer_name": ["Purdue Pharma L.P."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, GLASS in 1 CARTON (59011-960-10)  / 2 mL in 1 VIAL, GLASS", "package_ndc": "59011-960-10", "marketing_start_date": "20220208"}], "brand_name": "NALMEFENE HYDROCHLORIDE", "product_id": "59011-960_ec96ac7c-4d1f-4973-b7de-a7955acbd557", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "59011-960", "generic_name": "NALMEFENE HYDROCHLORIDE", "labeler_name": "Purdue Pharma L.P.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALMEFENE HYDROCHLORIDE", "active_ingredients": [{"name": "NALMEFENE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA212955", "marketing_category": "ANDA", "marketing_start_date": "20220208", "listing_expiration_date": "20261231"}