Package 71335-1917-3

{"route": ["ORAL"], "spl_id": "7da2dbe1-dd39-487c-99ee-59ff2fae4eb2", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923426"], "spl_set_id": ["2f13a6dd-dd77-47c8-ac5d-4a746c32dbd0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1917-1)", "package_ndc": "71335-1917-1", "marketing_start_date": "20220706"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1917-2)", "package_ndc": "71335-1917-2", "marketing_start_date": "20210722"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1917-3)", "package_ndc": "71335-1917-3", "marketing_start_date": "20210722"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1917-4)", "package_ndc": "71335-1917-4", "marketing_start_date": "20220706"}], "brand_name": "Sotalol Hydrochloride", "product_id": "71335-1917_7da2dbe1-dd39-487c-99ee-59ff2fae4eb2", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "71335-1917", "generic_name": "Sotalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA075563", "marketing_category": "ANDA", "marketing_start_date": "20200724", "listing_expiration_date": "20261231"}