Package 50090-4227-0

Brand: propafenone hydrochloride

Generic: propafenone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-4227-0
Digits Only 5009042270
Product NDC 50090-4227
Description

60 TABLET, COATED in 1 BOTTLE (50090-4227-0)

Marketing

Marketing Status
Marketed Since 2019-03-27
Brand propafenone hydrochloride
Generic propafenone hydrochloride
Sample Package No

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"}