Package 69238-2104-7
Brand: naloxone hydrochloride
Generic: naloxone hydrochloridePackage Facts
Identity
Package NDC
69238-2104-7
Digits Only
6923821047
Product NDC
69238-2104
Description
2 VIAL, SINGLE-DOSE in 1 CARTON (69238-2104-7) / .1 mL in 1 VIAL, SINGLE-DOSE (69238-2104-1)
Marketing
Marketing Status
Brand
naloxone hydrochloride
Generic
naloxone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "578cd3f4-d52a-46cb-bdca-88ab555be347", "openfda": {"upc": ["0369238210477"], "unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["8091a73d-9ecd-4578-a57b-5d85a2c5a16a"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (69238-2104-7) / .1 mL in 1 VIAL, SINGLE-DOSE (69238-2104-1)", "package_ndc": "69238-2104-7", "marketing_start_date": "20240424"}], "brand_name": "Naloxone Hydrochloride", "product_id": "69238-2104_578cd3f4-d52a-46cb-bdca-88ab555be347", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "69238-2104", "generic_name": "Naloxone Hydrochloride", "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"}