Package 71205-046-60

{"route": ["ORAL"], "spl_id": "8fd472ad-bdc0-4672-b67c-658ce12aafc0", "openfda": {"upc": ["0371205046309"], "unii": ["HEC37C70XX"], "rxcui": ["1923426"], "spl_set_id": ["6acf10b5-bbd9-4993-99a9-2cdb8cec96c5"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-046-30)", "package_ndc": "71205-046-30", "marketing_start_date": "20180601"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-046-60)", "package_ndc": "71205-046-60", "marketing_start_date": "20180601"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-046-90)", "package_ndc": "71205-046-90", "marketing_start_date": "20180601"}], "brand_name": "Sotalol Hydrochloride", "product_id": "71205-046_8fd472ad-bdc0-4672-b67c-658ce12aafc0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "71205-046", "generic_name": "Sotalol Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA075429", "marketing_category": "ANDA", "marketing_start_date": "20000504", "listing_expiration_date": "20261231"}