Package 11788-054-01
Brand: sotalol hydrochloride
Generic: sotalol hydrochloridePackage Facts
Identity
Package NDC
11788-054-01
Digits Only
1178805401
Product NDC
11788-054
Description
100 TABLET in 1 BOTTLE (11788-054-01)
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": "d2c31b08-0c64-48be-aa84-aeaead306b2a", "openfda": {"upc": ["0311788051017", "0311788052014"], "unii": ["HEC37C70XX"], "rxcui": ["904589", "1923422", "1923424", "1923426"], "spl_set_id": ["56326224-fc80-4b89-8ba3-70cb873173b4"], "manufacturer_name": ["AiPing Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (11788-054-01)", "package_ndc": "11788-054-01", "marketing_start_date": "20251101"}], "brand_name": "SOTALOL HYDROCHLORIDE", "product_id": "11788-054_d2c31b08-0c64-48be-aa84-aeaead306b2a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "11788-054", "generic_name": "SOTALOL HYDROCHLORIDE", "labeler_name": "AiPing Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SOTALOL HYDROCHLORIDE", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "240 mg/1"}], "application_number": "ANDA075500", "marketing_category": "ANDA", "marketing_start_date": "20251101", "listing_expiration_date": "20261231"}