Package 59651-258-01

Brand: propafenone hydrochloride

Generic: propafenone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59651-258-01
Digits Only 5965125801
Product NDC 59651-258
Product ID 59651-258_b59b252f-8b73-4f72-8d01-4d2076c18fa6
Description

100 TABLET, FILM COATED in 1 BOTTLE (59651-258-01)

Marketing

Marketing Status
Marketed Since 2019-10-25
Brand propafenone hydrochloride
Generic propafenone hydrochloride
Sample Package No

Linked Drug Pages (1)

PROPAFENONE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b59b252f-8b73-4f72-8d01-4d2076c18fa6", "openfda": {"unii": ["33XCH0HOCD"], "rxcui": ["861424", "861427", "861430"], "spl_set_id": ["0c887381-42fe-4f37-858a-d9ffb218dd1c"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-258-01)", "package_ndc": "59651-258-01", "marketing_start_date": "20191025"}], "brand_name": "PROPAFENONE HYDROCHLORIDE", "product_id": "59651-258_b59b252f-8b73-4f72-8d01-4d2076c18fa6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "59651-258", "generic_name": "PROPAFENONE HYDROCHLORIDE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPAFENONE HYDROCHLORIDE", "active_ingredients": [{"name": "PROPAFENONE HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA202445", "marketing_category": "ANDA", "marketing_start_date": "20191025", "listing_expiration_date": "20261231"}