sotalol hydrochloride

Generic: sotalol hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sotalol hydrochloride
Generic Name sotalol hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sotalol hydrochloride 80 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1299
Product ID 50090-1299_2b35de26-dca3-4508-b0c4-f9bdea0e41da
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076140
Listing Expiration 2026-12-31
Marketing Start 2003-02-01

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 500901299
Hyphenated Format 50090-1299

Supplemental Identifiers

RxCUI
1923426
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 ANDA076140 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (50090-1299-0)
  • 30 TABLET in 1 BOTTLE (50090-1299-1)
  • 90 TABLET in 1 BOTTLE (50090-1299-2)
source: ndc

Packages (3)

50090-1299-0 60 TABLET in 1 BOTTLE (50090-1299-0) 50090-1299-1 30 TABLET in 1 BOTTLE (50090-1299-1) 50090-1299-2 90 TABLET in 1 BOTTLE (50090-1299-2)

Ingredients (1)

sotalol hydrochloride (80 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": "2b35de26-dca3-4508-b0c4-f9bdea0e41da", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923426"], "spl_set_id": ["7cb4879f-31e7-4862-bc0c-d439e592d81c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-1299-0)", "package_ndc": "50090-1299-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-1299-1)", "package_ndc": "50090-1299-1", "marketing_start_date": "20220202"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-1299-2)", "package_ndc": "50090-1299-2", "marketing_start_date": "20201104"}], "brand_name": "Sotalol Hydrochloride", "product_id": "50090-1299_2b35de26-dca3-4508-b0c4-f9bdea0e41da", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "50090-1299", "generic_name": "Sotalol Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA076140", "marketing_category": "ANDA", "marketing_start_date": "20030201", "listing_expiration_date": "20261231"}