Package 76385-115-50

Brand: sotalol

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76385-115-50
Digits Only 7638511550
Product NDC 76385-115
Description

500 TABLET in 1 BOTTLE, PLASTIC (76385-115-50)

Marketing

Marketing Status
Marketed Since 2017-12-06
Brand sotalol
Generic sotalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fe9ac463-547d-4917-a98e-61f1c0fe38f1", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1922720", "1922763", "1922765", "1923422", "1923424", "1923426"], "spl_set_id": ["56879738-8662-4f5c-8386-761ab2b5e46f"], "manufacturer_name": ["UNICHEM PHARMACEUTICALS (USA), INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (76385-115-01)", "package_ndc": "76385-115-01", "marketing_start_date": "20171215"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (76385-115-50)", "package_ndc": "76385-115-50", "marketing_start_date": "20171206"}], "brand_name": "Sotalol", "product_id": "76385-115_fe9ac463-547d-4917-a98e-61f1c0fe38f1", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "76385-115", "generic_name": "Sotalol Hydrochloride", "labeler_name": "UNICHEM PHARMACEUTICALS (USA), INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA207428", "marketing_category": "ANDA", "marketing_start_date": "20171206", "listing_expiration_date": "20271231"}