Package 71335-2419-5

{"route": ["ORAL"], "spl_id": "e0afc24e-ee9e-4321-bf71-85e84772d1e9", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["d7ba0156-6222-4619-a043-b5a1342d5375"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2419-1)", "package_ndc": "71335-2419-1", "marketing_start_date": "20241112"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2419-2)", "package_ndc": "71335-2419-2", "marketing_start_date": "20241112"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2419-3)", "package_ndc": "71335-2419-3", "marketing_start_date": "20241112"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71335-2419-4)", "package_ndc": "71335-2419-4", "marketing_start_date": "20241112"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-2419-5)", "package_ndc": "71335-2419-5", "marketing_start_date": "20241112"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-2419-6)", "package_ndc": "71335-2419-6", "marketing_start_date": "20241112"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-2419-7)", "package_ndc": "71335-2419-7", "marketing_start_date": "20241112"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "71335-2419_e0afc24e-ee9e-4321-bf71-85e84772d1e9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71335-2419", "generic_name": "Naltrexone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naltrexone Hydrochloride", "active_ingredients": [{"name": "NALTREXONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075274", "marketing_category": "ANDA", "marketing_start_date": "20240215", "listing_expiration_date": "20261231"}