Package 0641-6260-25

Brand: naloxone hydrochloride

Generic: nalxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0641-6260-25
Digits Only 0641626025
Product NDC 0641-6260
Product ID 0641-6260_531da15c-9a2c-4121-9aa5-85b079d3908b
Description

25 VIAL in 1 CARTON (0641-6260-25) / 1 mL in 1 VIAL (0641-6260-01)

Marketing

Marketing Status
Marketed Since 2022-03-01
Brand naloxone hydrochloride
Generic nalxone 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": "531da15c-9a2c-4121-9aa5-85b079d3908b", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["1bef59b9-7d51-4f19-a054-44b8eb6c6398"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0641-6260-25)  / 1 mL in 1 VIAL (0641-6260-01)", "package_ndc": "0641-6260-25", "marketing_start_date": "20220301"}], "brand_name": "Naloxone Hydrochloride", "product_id": "0641-6260_531da15c-9a2c-4121-9aa5-85b079d3908b", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0641-6260", "generic_name": "Nalxone Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA070299", "marketing_category": "ANDA", "marketing_start_date": "20220301", "listing_expiration_date": "20261231"}