Package 51655-450-15

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-450-15
Digits Only 5165545015
Product NDC 51655-450
Product ID 51655-450_490ece67-ce5a-8020-e063-6394a90a9bac
Description

50 TABLET in 1 BOTTLE, PLASTIC (51655-450-15)

Marketing

Marketing Status
Marketed Since 2023-06-14
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": "490ece67-ce5a-8020-e063-6394a90a9bac", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["904589"], "spl_set_id": ["fe82c866-03d4-e07b-e053-6394a90a8b1e"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (51655-450-15)", "package_ndc": "51655-450-15", "marketing_start_date": "20230614"}], "brand_name": "Sotalol Hydrochloride", "product_id": "51655-450_490ece67-ce5a-8020-e063-6394a90a9bac", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "51655-450", "generic_name": "Sotalol Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "240 mg/1"}], "application_number": "ANDA076140", "marketing_category": "ANDA", "marketing_start_date": "20230614", "listing_expiration_date": "20271231"}