Package 72162-1932-1

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1932-1
Digits Only 7216219321
Product NDC 72162-1932
Product ID 72162-1932_0fd4afc7-dbf8-46be-9657-aa83bbb2c026
Description

100 TABLET in 1 BOTTLE (72162-1932-1)

Marketing

Marketing Status
Marketed Since 2020-07-24
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": "0fd4afc7-dbf8-46be-9657-aa83bbb2c026", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923422"], "spl_set_id": ["0fd4afc7-dbf8-46be-9657-aa83bbb2c026"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1932-1)", "package_ndc": "72162-1932-1", "marketing_start_date": "20200724"}], "brand_name": "Sotalol Hydrochloride", "product_id": "72162-1932_0fd4afc7-dbf8-46be-9657-aa83bbb2c026", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "72162-1932", "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": "120 mg/1"}], "application_number": "ANDA075563", "marketing_category": "ANDA", "marketing_start_date": "20200724", "listing_expiration_date": "20261231"}