Package 42806-123-10
Brand: sotalol hydrochloride
Generic: sotalol hydrochloridePackage Facts
Identity
Package NDC
42806-123-10
Digits Only
4280612310
Product NDC
42806-123
Description
1000 TABLET in 1 BOTTLE (42806-123-10)
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": "34ed0846-81bd-46c4-a57c-b617c7d8232d", "openfda": {"upc": ["0342806121016", "0342806122013"], "unii": ["HEC37C70XX"], "rxcui": ["1922720", "1922763", "1922765"], "spl_set_id": ["c0a34c56-9641-4592-9754-bcc233ec86b6"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-123-01)", "package_ndc": "42806-123-01", "marketing_start_date": "20160104"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (42806-123-10)", "package_ndc": "42806-123-10", "marketing_start_date": "20160104"}], "brand_name": "Sotalol hydrochloride", "product_id": "42806-123_34ed0846-81bd-46c4-a57c-b617c7d8232d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "42806-123", "generic_name": "sotalol hydrochloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "160 mg/1"}], "application_number": "ANDA077070", "marketing_category": "ANDA", "marketing_start_date": "20160104", "listing_expiration_date": "20261231"}