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 120 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-2423
Product ID
63629-2423_83bf1c37-e5b7-47a9-9e04-cf3324048fc3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075563
Listing Expiration
2026-12-31
Marketing Start
2020-07-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636292423
Hyphenated Format
63629-2423
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
ANDA075563 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 120 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (63629-2423-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "83bf1c37-e5b7-47a9-9e04-cf3324048fc3", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923422"], "spl_set_id": ["9a36d95c-6e93-4e57-befe-b5274f359244"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-2423-1)", "package_ndc": "63629-2423-1", "marketing_start_date": "20200724"}], "brand_name": "Sotalol Hydrochloride", "product_id": "63629-2423_83bf1c37-e5b7-47a9-9e04-cf3324048fc3", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "63629-2423", "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": "120 mg/1"}], "application_number": "ANDA075563", "marketing_category": "ANDA", "marketing_start_date": "20200724", "listing_expiration_date": "20261231"}