Package 72162-2522-1

Brand: sotalol

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2522-1
Digits Only 7216225221
Product NDC 72162-2522
Product ID 72162-2522_c1b87a0a-b217-431f-8aa0-6ede44e51ce6
Description

100 TABLET in 1 BOTTLE (72162-2522-1)

Marketing

Marketing Status
Marketed Since 2025-07-11
Brand sotalol
Generic sotalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Sotalol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c1b87a0a-b217-431f-8aa0-6ede44e51ce6", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923422"], "spl_set_id": ["51cebe16-4496-4f49-b2db-b7b21c08fa23"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2522-1)", "package_ndc": "72162-2522-1", "marketing_start_date": "20250711"}], "brand_name": "Sotalol", "product_id": "72162-2522_c1b87a0a-b217-431f-8aa0-6ede44e51ce6", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "72162-2522", "generic_name": "Sotalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA207428", "marketing_category": "ANDA", "marketing_start_date": "20171206", "listing_expiration_date": "20261231"}