Package 71610-723-30

{"route": ["ORAL"], "spl_id": "15689e23-7236-4cfd-8ab4-9b8450b82299", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923426"], "spl_set_id": ["5e005309-4eca-4536-8743-c6ed9e5b3195"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71610-723-30)", "package_ndc": "71610-723-30", "marketing_start_date": "20230807"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-723-60)", "package_ndc": "71610-723-60", "marketing_start_date": "20230807"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71610-723-80)", "package_ndc": "71610-723-80", "marketing_start_date": "20230807"}], "brand_name": "Sotalol Hydrochloride", "product_id": "71610-723_15689e23-7236-4cfd-8ab4-9b8450b82299", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "71610-723", "generic_name": "Sotalol Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA076140", "marketing_category": "ANDA", "marketing_start_date": "20020926", "listing_expiration_date": "20261231"}