Package 69584-843-10

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69584-843-10
Digits Only 6958484310
Product NDC 69584-843
Product ID 69584-843_71c67f34-73e1-4e4c-9c72-56f4b9222a88
Description

100 TABLET in 1 BOTTLE (69584-843-10)

Marketing

Marketing Status
Marketed Since 2020-07-24
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": "71c67f34-73e1-4e4c-9c72-56f4b9222a88", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["904589", "1923422", "1923424", "1923426"], "spl_set_id": ["c8ac6351-b1e9-4dd2-82f2-5980814fda15"], "manufacturer_name": ["Oxford Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69584-843-10)", "package_ndc": "69584-843-10", "marketing_start_date": "20200724"}], "brand_name": "Sotalol Hydrochloride", "product_id": "69584-843_71c67f34-73e1-4e4c-9c72-56f4b9222a88", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "69584-843", "generic_name": "Sotalol Hydrochloride", "labeler_name": "Oxford Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "160 mg/1"}], "application_number": "ANDA075563", "marketing_category": "ANDA", "marketing_start_date": "20200724", "listing_expiration_date": "20261231"}