Package 0904-7143-61

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7143-61
Digits Only 0904714361
Product NDC 0904-7143
Product ID 0904-7143_2b64f084-8d8f-454c-834b-16e8d1439c77
Description

100 BLISTER PACK in 1 CARTON (0904-7143-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2003-02-01
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": "2b64f084-8d8f-454c-834b-16e8d1439c77", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923426"], "spl_set_id": ["866e5717-3de2-4f19-b7c7-2275caeef78b"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7143-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7143-61", "marketing_start_date": "20030201"}], "brand_name": "Sotalol Hydrochloride", "product_id": "0904-7143_2b64f084-8d8f-454c-834b-16e8d1439c77", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "0904-7143", "generic_name": "Sotalol Hydrochloride", "labeler_name": "Major Pharmaceuticals", "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": "20030201", "listing_expiration_date": "20261231"}