Package 60505-0081-1

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60505-0081-1
Digits Only 6050500811
Product NDC 60505-0081
Description

1000 TABLET in 1 BOTTLE (60505-0081-1)

Marketing

Marketing Status
Marketed Since 2003-02-01
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": "7e1fd07e-45aa-ef32-da1b-c81f6961f216", "openfda": {"upc": ["0360505015900", "0360505008209"], "unii": ["HEC37C70XX"], "rxcui": ["904589", "1922720", "1922763", "1922765", "1923422", "1923424", "1923426"], "spl_set_id": ["1a56c82e-7ecd-43b0-2899-f89e47adf7db"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (60505-0081-0)", "package_ndc": "60505-0081-0", "marketing_start_date": "20030201"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (60505-0081-1)", "package_ndc": "60505-0081-1", "marketing_start_date": "20030201"}], "brand_name": "Sotalol Hydrochloride", "product_id": "60505-0081_7e1fd07e-45aa-ef32-da1b-c81f6961f216", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "60505-0081", "generic_name": "Sotalol Hydrochloride", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "160 mg/1"}], "application_number": "ANDA076140", "marketing_category": "ANDA", "marketing_start_date": "20030201", "listing_expiration_date": "20261231"}