Package 59651-776-01

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59651-776-01
Digits Only 5965177601
Product NDC 59651-776
Product ID 59651-776_8a142042-e510-4232-8f20-5c92a991bd91
Description

100 TABLET in 1 BOTTLE (59651-776-01)

Marketing

Marketing Status
Marketed Since 2023-06-29
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": "8a142042-e510-4232-8f20-5c92a991bd91", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1922720", "1922763", "1922765"], "spl_set_id": ["6f3145d7-f3c9-4456-a77d-d04c54f24668"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-776-01)", "package_ndc": "59651-776-01", "marketing_start_date": "20230629"}], "brand_name": "SOTALOL HYDROCHLORIDE", "product_id": "59651-776_8a142042-e510-4232-8f20-5c92a991bd91", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "59651-776", "generic_name": "SOTALOL HYDROCHLORIDE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SOTALOL HYDROCHLORIDE", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA077616", "marketing_category": "ANDA", "marketing_start_date": "20230629", "listing_expiration_date": "20261231"}