Package 67296-1928-2
Brand: naloxone hydrochloride
Generic: naloxone hydrochloridePackage Facts
Identity
Package NDC
67296-1928-2
Digits Only
6729619282
Product NDC
67296-1928
Description
2 BLISTER PACK in 1 CARTON (67296-1928-2) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK / .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": "46e9401c-067d-0ed9-e063-6294a90aca49", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["2fc0a205-6075-6253-e063-6294a90ad2df"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (67296-1928-2) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "67296-1928-2", "marketing_end_date": "20260630", "marketing_start_date": "20211222"}], "brand_name": "Naloxone Hydrochloride", "product_id": "67296-1928_46e9401c-067d-0ed9-e063-6294a90aca49", "dosage_form": "SPRAY, METERED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "67296-1928", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA209522", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20211222"}