Package 0480-3478-68
Brand: naloxone hydrochloride
Generic: naloxone hydrochloridePackage Facts
Identity
Package NDC
0480-3478-68
Digits Only
0480347868
Product NDC
0480-3478
Description
2 BLISTER PACK in 1 CARTON (0480-3478-68) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK (0480-3478-19) / .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": "7545d296-ad3c-4be1-9913-73b4f870e90c", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["3a73ee4b-c2a4-496f-be90-9f78c8046062"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0480-3478-68) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK (0480-3478-19) / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0480-3478-68", "marketing_start_date": "20240923"}], "brand_name": "Naloxone Hydrochloride", "product_id": "0480-3478_7545d296-ad3c-4be1-9913-73b4f870e90c", "dosage_form": "SPRAY, METERED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0480-3478", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Teva Pharmaceuticals, 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": "20240923", "listing_expiration_date": "20261231"}