Package 0591-3871-99
Brand: naloxone hydrochloride
Generic: naloxone hydrochloridePackage Facts
Identity
Package NDC
0591-3871-99
Digits Only
0591387199
Product NDC
0591-3871
Description
2 BLISTER PACK in 1 CARTON (0591-3871-99) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK (0591-3871-54) / .1 mL in 1 VIAL, SINGLE-DOSE
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": "2c4bb622-fc96-4877-92c8-a15be1636137", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["49350f7e-d613-40a8-8941-a2ec30eafdf3"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0591-3871-99) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK (0591-3871-54) / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0591-3871-99", "marketing_start_date": "20250117"}], "brand_name": "Naloxone Hydrochloride", "product_id": "0591-3871_2c4bb622-fc96-4877-92c8-a15be1636137", "dosage_form": "SPRAY, METERED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0591-3871", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA209522", "marketing_category": "ANDA", "marketing_start_date": "20250117", "listing_expiration_date": "20261231"}