Package 60429-748-01

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60429-748-01
Digits Only 6042974801
Product NDC 60429-748
Description

100 TABLET in 1 BOTTLE (60429-748-01)

Marketing

Marketing Status
Marketed Since 2003-02-01
Brand sotalol hydrochloride
Generic sotalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c55fac0-8327-5685-e063-6294a90a6292", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["904589", "1923422", "1923424", "1923426"], "spl_set_id": ["6674d53a-7137-4822-8841-4982f702a1b8"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (60429-748-01)", "package_ndc": "60429-748-01", "marketing_start_date": "20030201"}], "brand_name": "Sotalol Hydrochloride", "product_id": "60429-748_3c55fac0-8327-5685-e063-6294a90a6292", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "60429-748", "generic_name": "Sotalol Hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "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": "20020926", "listing_expiration_date": "20261231"}