Package 72162-1931-1

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1931-1
Digits Only 7216219311
Product NDC 72162-1931
Product ID 72162-1931_89b33c45-ece8-496f-9c3a-94ebabf73b1b
Description

100 TABLET in 1 BOTTLE (72162-1931-1)

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": "89b33c45-ece8-496f-9c3a-94ebabf73b1b", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923426"], "spl_set_id": ["89b33c45-ece8-496f-9c3a-94ebabf73b1b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1931-1)", "package_ndc": "72162-1931-1", "marketing_start_date": "20200724"}], "brand_name": "Sotalol Hydrochloride", "product_id": "72162-1931_89b33c45-ece8-496f-9c3a-94ebabf73b1b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "72162-1931", "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"}