sotalol hydrochloride
Generic: sotalol hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
sotalol hydrochloride
Generic Name
sotalol hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
sotalol hydrochloride 240 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2586
Product ID
72162-2586_ae310c7a-e269-4e9e-ae4c-2103f4b4c637
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075500
Listing Expiration
2026-12-31
Marketing Start
2025-11-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622586
Hyphenated Format
72162-2586
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
sotalol hydrochloride (source: ndc)
Generic Name
sotalol hydrochloride (source: ndc)
Application Number
ANDA075500 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 240 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (72162-2586-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ae310c7a-e269-4e9e-ae4c-2103f4b4c637", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["904589"], "spl_set_id": ["56dd490f-4d78-447c-a460-f55587e8a764"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2586-1)", "package_ndc": "72162-2586-1", "marketing_start_date": "20251124"}], "brand_name": "SOTALOL HYDROCHLORIDE", "product_id": "72162-2586_ae310c7a-e269-4e9e-ae4c-2103f4b4c637", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "72162-2586", "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": "240 mg/1"}], "application_number": "ANDA075500", "marketing_category": "ANDA", "marketing_start_date": "20251101", "listing_expiration_date": "20261231"}