Package 72162-2585-1

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2585-1
Digits Only 7216225851
Product NDC 72162-2585
Product ID 72162-2585_f97f710d-0bbb-489a-9c5b-7d41d66edaa8
Description

100 TABLET in 1 BOTTLE (72162-2585-1)

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": "f97f710d-0bbb-489a-9c5b-7d41d66edaa8", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923424"], "spl_set_id": ["db9b0b36-4c00-45b6-a50a-e08d7c61a17c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2585-1)", "package_ndc": "72162-2585-1", "marketing_start_date": "20251124"}], "brand_name": "SOTALOL HYDROCHLORIDE", "product_id": "72162-2585_f97f710d-0bbb-489a-9c5b-7d41d66edaa8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "72162-2585", "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": "160 mg/1"}], "application_number": "ANDA075500", "marketing_category": "ANDA", "marketing_start_date": "20251101", "listing_expiration_date": "20261231"}