Package 51662-1620-1
Brand: naloxone hcl
Generic: naloxone hclPackage Facts
Identity
Package NDC
51662-1620-1
Digits Only
5166216201
Product NDC
51662-1620
Description
.1 mL in 1 VIAL, SINGLE-DOSE (51662-1620-1)
Marketing
Marketing Status
Brand
naloxone hcl
Generic
naloxone hcl
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "100bc933-5bf3-8de2-e063-6294a90a7ba6", "openfda": {"upc": ["0345802811004"], "unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["f8fcda15-8ba6-e66a-e053-6294a90a385c"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": ".1 mL in 1 VIAL, SINGLE-DOSE (51662-1620-1)", "package_ndc": "51662-1620-1", "marketing_start_date": "20230410"}, {"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (51662-1620-2) / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51662-1620-2", "marketing_start_date": "20230410"}], "brand_name": "NALOXONE HCl", "product_id": "51662-1620_100bc933-5bf3-8de2-e063-6294a90a7ba6", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "51662-1620", "generic_name": "NALOXONE HCl", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALOXONE HCl", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA211951", "marketing_category": "ANDA", "marketing_start_date": "20230410", "listing_expiration_date": "20261231"}