propafenone hydrochloride
Generic: propafenone hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
propafenone hydrochloride
Generic Name
propafenone hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET, COATED
Routes
Active Ingredients
propafenone hydrochloride 225 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-4227
Product ID
50090-4227_f85edfc7-e69c-45ec-b7c0-190c6565e704
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076550
Listing Expiration
2026-12-31
Marketing Start
2015-03-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500904227
Hyphenated Format
50090-4227
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
propafenone hydrochloride (source: ndc)
Generic Name
propafenone hydrochloride (source: ndc)
Application Number
ANDA076550 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 225 mg/1
Packaging
- 60 TABLET, COATED in 1 BOTTLE (50090-4227-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f85edfc7-e69c-45ec-b7c0-190c6565e704", "openfda": {"unii": ["33XCH0HOCD"], "rxcui": ["861427"], "spl_set_id": ["41b4e503-60a6-4662-a6f9-46ecf93d930a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (50090-4227-0)", "package_ndc": "50090-4227-0", "marketing_start_date": "20190327"}], "brand_name": "Propafenone Hydrochloride", "product_id": "50090-4227_f85edfc7-e69c-45ec-b7c0-190c6565e704", "dosage_form": "TABLET, COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "50090-4227", "generic_name": "Propafenone Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propafenone Hydrochloride", "active_ingredients": [{"name": "PROPAFENONE HYDROCHLORIDE", "strength": "225 mg/1"}], "application_number": "ANDA076550", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}