Package 71335-2823-1

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2823-1
Digits Only 7133528231
Product NDC 71335-2823
Product ID 71335-2823_8aaf8e38-d3f0-4ba6-8168-21b978532601
Description

100 TABLET in 1 BOTTLE (71335-2823-1)

Marketing

Marketing Status
Marketed Since 2025-11-10
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": "8aaf8e38-d3f0-4ba6-8168-21b978532601", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923426"], "spl_set_id": ["d6c8f659-1c32-4431-bdb2-3211a1c81006"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2823-1)", "package_ndc": "71335-2823-1", "marketing_start_date": "20251110"}], "brand_name": "Sotalol Hydrochloride", "product_id": "71335-2823_8aaf8e38-d3f0-4ba6-8168-21b978532601", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "71335-2823", "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": "80 mg/1"}], "application_number": "ANDA075563", "marketing_category": "ANDA", "marketing_start_date": "20200724", "listing_expiration_date": "20261231"}