Package 63629-2423-1

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2423-1
Digits Only 6362924231
Product NDC 63629-2423
Description

100 TABLET in 1 BOTTLE (63629-2423-1)

Marketing

Marketing Status
Marketed Since 2020-07-24
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": "83bf1c37-e5b7-47a9-9e04-cf3324048fc3", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923422"], "spl_set_id": ["9a36d95c-6e93-4e57-befe-b5274f359244"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-2423-1)", "package_ndc": "63629-2423-1", "marketing_start_date": "20200724"}], "brand_name": "Sotalol Hydrochloride", "product_id": "63629-2423_83bf1c37-e5b7-47a9-9e04-cf3324048fc3", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "63629-2423", "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": "120 mg/1"}], "application_number": "ANDA075563", "marketing_category": "ANDA", "marketing_start_date": "20200724", "listing_expiration_date": "20261231"}