Package 63629-1989-1

Brand: propafenone hydrochloride

Generic: propafenone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1989-1
Digits Only 6362919891
Product NDC 63629-1989
Product ID 63629-1989_1a40d563-a1f1-4a18-b7db-b6a460f0a33d
Description

100 TABLET, COATED in 1 BOTTLE (63629-1989-1)

Marketing

Marketing Status
Marketed Since 2021-02-02
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": "1a40d563-a1f1-4a18-b7db-b6a460f0a33d", "openfda": {"unii": ["33XCH0HOCD"], "rxcui": ["861430"], "spl_set_id": ["7bcc5d3b-b2c9-4753-9eef-b5360538f5ee"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (63629-1989-1)", "package_ndc": "63629-1989-1", "marketing_start_date": "20210202"}], "brand_name": "Propafenone Hydrochloride", "product_id": "63629-1989_1a40d563-a1f1-4a18-b7db-b6a460f0a33d", "dosage_form": "TABLET, COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "63629-1989", "generic_name": "Propafenone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propafenone Hydrochloride", "active_ingredients": [{"name": "PROPAFENONE HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA076550", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}