Package 60219-2104-7

Brand: naloxone hydrochloride

Generic: naloxone
NDC Package

Package Facts

Identity

Package NDC 60219-2104-7
Digits Only 6021921047
Product NDC 60219-2104
Product ID 60219-2104_a79738c5-1989-43c7-856b-f284c654c9c0
Description

2 VIAL in 1 CARTON (60219-2104-7) / .1 mL in 1 VIAL (60219-2104-1)

Marketing

Marketing Status
Marketed Since 2024-04-24
Brand naloxone hydrochloride
Generic naloxone
Sample Package No

Linked Drug Pages (1)

Naloxone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "a79738c5-1989-43c7-856b-f284c654c9c0", "openfda": {"upc": ["0360219210479"], "unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["8779a073-dc6e-410a-9959-fd370f0079f9"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL in 1 CARTON (60219-2104-7)  / .1 mL in 1 VIAL (60219-2104-1)", "package_ndc": "60219-2104-7", "marketing_start_date": "20240424"}], "brand_name": "Naloxone Hydrochloride", "product_id": "60219-2104_a79738c5-1989-43c7-856b-f284c654c9c0", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "60219-2104", "generic_name": "Naloxone", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA217992", "marketing_category": "ANDA", "marketing_start_date": "20240424", "listing_expiration_date": "20271231"}