Package 82804-974-11
Brand: sotalol hydrochloride
Generic: sotalol hydrochloridePackage Facts
Identity
Package NDC
82804-974-11
Digits Only
8280497411
Product NDC
82804-974
Description
1000 TABLET in 1 BOTTLE (82804-974-11)
Marketing
Marketing Status
Brand
sotalol hydrochloride
Generic
sotalol hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "959dc952-bed6-4538-a1a6-61ed10c06be4", "openfda": {"upc": ["0382804974306"], "unii": ["HEC37C70XX"], "rxcui": ["1923426"], "spl_set_id": ["b534c632-3b67-4812-a045-3e582eda6de4"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82804-974-00)", "package_ndc": "82804-974-00", "marketing_start_date": "20250213"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (82804-974-11)", "package_ndc": "82804-974-11", "marketing_start_date": "20250213"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-974-30)", "package_ndc": "82804-974-30", "marketing_start_date": "20250213"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (82804-974-55)", "package_ndc": "82804-974-55", "marketing_start_date": "20250213"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-974-60)", "package_ndc": "82804-974-60", "marketing_start_date": "20250213"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (82804-974-72)", "package_ndc": "82804-974-72", "marketing_start_date": "20250213"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-974-90)", "package_ndc": "82804-974-90", "marketing_start_date": "20250213"}], "brand_name": "Sotalol Hydrochloride", "product_id": "82804-974_959dc952-bed6-4538-a1a6-61ed10c06be4", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "82804-974", "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": "ANDA075563", "marketing_category": "ANDA", "marketing_start_date": "20200724", "listing_expiration_date": "20261231"}