Package 72789-135-01
Brand: sotalol hydrochloride
Generic: sotalol hydrochloridePackage Facts
Identity
Package NDC
72789-135-01
Digits Only
7278913501
Product NDC
72789-135
Description
100 TABLET in 1 BOTTLE, PLASTIC (72789-135-01)
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": "40a68ec8-c1d1-cc50-e063-6394a90aacca", "openfda": {"upc": ["0372789137018", "0372789138015", "0372789136011", "0372789135014"], "unii": ["HEC37C70XX"], "rxcui": ["904589", "1923422", "1923424", "1923426"], "spl_set_id": ["e6ea445d-4d7c-4c32-83a7-e7683a56075b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-135-01)", "package_ndc": "72789-135-01", "marketing_start_date": "20201106"}], "brand_name": "Sotalol Hydrochloride", "product_id": "72789-135_40a68ec8-c1d1-cc50-e063-6394a90aacca", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "72789-135", "generic_name": "Sotalol Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "160 mg/1"}], "application_number": "ANDA075563", "marketing_category": "ANDA", "marketing_start_date": "20200724", "listing_expiration_date": "20261231"}