Package 50268-725-15

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-725-15
Digits Only 5026872515
Product NDC 50268-725
Product ID 50268-725_47fc0908-1c7a-abc6-e063-6294a90a20b2
Description

50 BLISTER PACK in 1 BOX (50268-725-15) / 1 TABLET in 1 BLISTER PACK (50268-725-11)

Marketing

Marketing Status
Marketed Since 2021-03-04
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": "47fc0908-1c7a-abc6-e063-6294a90a20b2", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923422", "1923426"], "spl_set_id": ["bcbc1624-283e-732f-e053-2995a90a8f11"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-725-15)  / 1 TABLET in 1 BLISTER PACK (50268-725-11)", "package_ndc": "50268-725-15", "marketing_start_date": "20210304"}], "brand_name": "Sotalol Hydrochloride", "product_id": "50268-725_47fc0908-1c7a-abc6-e063-6294a90a20b2", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "50268-725", "generic_name": "Sotalol Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA076140", "marketing_category": "ANDA", "marketing_start_date": "20210304", "listing_expiration_date": "20271231"}