Package 50090-7796-0

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7796-0
Digits Only 5009077960
Product NDC 50090-7796
Description

60 TABLET in 1 BOTTLE (50090-7796-0)

Marketing

Marketing Status
Marketed Since 2025-11-25
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": "4d187dd3-c6fd-4e9a-a56a-b42b9f1d8882", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923426"], "spl_set_id": ["bbeaba9f-0513-4980-bc29-7f9259a53ecc"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-7796-0)", "package_ndc": "50090-7796-0", "marketing_start_date": "20251125"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7796-2)", "package_ndc": "50090-7796-2", "marketing_start_date": "20251203"}], "brand_name": "Sotalol Hydrochloride", "product_id": "50090-7796_4d187dd3-c6fd-4e9a-a56a-b42b9f1d8882", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "50090-7796", "generic_name": "Sotalol Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA075563", "marketing_category": "ANDA", "marketing_start_date": "20200724", "listing_expiration_date": "20261231"}