Package 63629-2422-1
Brand: sotalol hydrochloride
Generic: sotalol hydrochloridePackage Facts
Identity
Package NDC
63629-2422-1
Digits Only
6362924221
Product NDC
63629-2422
Description
100 TABLET in 1 BOTTLE (63629-2422-1)
Marketing
Marketing Status
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": "a15bc4c8-c35a-4805-9a97-ff5cf80758bb", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923426"], "spl_set_id": ["667fc1f2-6ccf-4373-89d8-6a064ee7509e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-2422-1)", "package_ndc": "63629-2422-1", "marketing_start_date": "20200724"}], "brand_name": "Sotalol Hydrochloride", "product_id": "63629-2422_a15bc4c8-c35a-4805-9a97-ff5cf80758bb", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "63629-2422", "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": "20271231"}