Package 72162-1626-1

{"route": ["ORAL"], "spl_id": "6bd63cd9-e21c-4cb0-a65c-31b696092e2f", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198223"], "spl_set_id": ["cbc817de-5ea8-4139-9c13-02bac8ff93c3"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-1626-1)", "package_ndc": "72162-1626-1", "marketing_start_date": "20230602"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-1626-3)", "package_ndc": "72162-1626-3", "marketing_start_date": "20230602"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-1626-5)", "package_ndc": "72162-1626-5", "marketing_start_date": "20230602"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72162-1626-6)", "package_ndc": "72162-1626-6", "marketing_start_date": "20230602"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72162-1626-9)", "package_ndc": "72162-1626-9", "marketing_start_date": "20230602"}], "brand_name": "SPIRONOLACTONE", "product_id": "72162-1626_6bd63cd9-e21c-4cb0-a65c-31b696092e2f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "72162-1626", "generic_name": "SPIRONOLACTONE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SPIRONOLACTONE", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "50 mg/1"}], "application_number": "ANDA089424", "marketing_category": "ANDA", "marketing_start_date": "19860723", "listing_expiration_date": "20261231"}