Package 71610-849-80

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-849-80
Digits Only 7161084980
Product NDC 71610-849
Product ID 71610-849_1f2ee516-a618-876f-e063-6394a90a3114
Description

180 TABLET in 1 BOTTLE (71610-849-80)

Marketing

Marketing Status
Marketed Since 2024-08-07
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": "1f2ee516-a618-876f-e063-6394a90a3114", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923426"], "spl_set_id": ["1f2ee505-eb90-885d-e063-6394a90a46a1"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE (71610-849-80)", "package_ndc": "71610-849-80", "marketing_start_date": "20240807"}], "brand_name": "Sotalol Hydrochloride", "product_id": "71610-849_1f2ee516-a618-876f-e063-6394a90a3114", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "71610-849", "generic_name": "Sotalol Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA076140", "marketing_category": "ANDA", "marketing_start_date": "20030201", "listing_expiration_date": "20261231"}