Package 72162-2586-1

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2586-1
Digits Only 7216225861
Product NDC 72162-2586
Product ID 72162-2586_ae310c7a-e269-4e9e-ae4c-2103f4b4c637
Description

100 TABLET in 1 BOTTLE (72162-2586-1)

Marketing

Marketing Status
Marketed Since 2025-11-24
Brand sotalol hydrochloride
Generic sotalol hydrochloride
Sample Package No

Linked Drug Pages (1)

SOTALOL HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ae310c7a-e269-4e9e-ae4c-2103f4b4c637", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["904589"], "spl_set_id": ["56dd490f-4d78-447c-a460-f55587e8a764"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2586-1)", "package_ndc": "72162-2586-1", "marketing_start_date": "20251124"}], "brand_name": "SOTALOL HYDROCHLORIDE", "product_id": "72162-2586_ae310c7a-e269-4e9e-ae4c-2103f4b4c637", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "72162-2586", "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": "240 mg/1"}], "application_number": "ANDA075500", "marketing_category": "ANDA", "marketing_start_date": "20251101", "listing_expiration_date": "20261231"}