sotalol hydrochloride

Generic: sotalol hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sotalol hydrochloride
Generic Name sotalol hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sotalol hydrochloride 160 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2585
Product ID 72162-2585_f97f710d-0bbb-489a-9c5b-7d41d66edaa8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075500
Listing Expiration 2026-12-31
Marketing Start 2025-11-01

Pharmacologic Class

Classes
adrenergic beta-antagonists [moa] antiarrhythmic [epc] cardiac rhythm alteration [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622585
Hyphenated Format 72162-2585

Supplemental Identifiers

RxCUI
1923424
UNII
HEC37C70XX

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72162-2585-1)
source: ndc

Packages (1)

72162-2585-1 100 TABLET in 1 BOTTLE (72162-2585-1)

Ingredients (1)

sotalol hydrochloride (160 mg/1)

Linked Drug Pages (1)

SOTALOL HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f97f710d-0bbb-489a-9c5b-7d41d66edaa8", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923424"], "spl_set_id": ["db9b0b36-4c00-45b6-a50a-e08d7c61a17c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2585-1)", "package_ndc": "72162-2585-1", "marketing_start_date": "20251124"}], "brand_name": "SOTALOL HYDROCHLORIDE", "product_id": "72162-2585_f97f710d-0bbb-489a-9c5b-7d41d66edaa8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "72162-2585", "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": "160 mg/1"}], "application_number": "ANDA075500", "marketing_category": "ANDA", "marketing_start_date": "20251101", "listing_expiration_date": "20261231"}