Package 63629-1988-1
Brand: propafenone hydrochloride
Generic: propafenone hydrochloridePackage Facts
Identity
Package NDC
63629-1988-1
Digits Only
6362919881
Product NDC
63629-1988
Description
100 TABLET, COATED in 1 BOTTLE (63629-1988-1)
Marketing
Marketing Status
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": "ff1cd958-1b7d-422c-bdfd-0fad7d98d6bc", "openfda": {"unii": ["33XCH0HOCD"], "rxcui": ["861427"], "spl_set_id": ["2492317c-8b04-477e-a5d2-53e791fface9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (63629-1988-1)", "package_ndc": "63629-1988-1", "marketing_start_date": "20210202"}], "brand_name": "Propafenone Hydrochloride", "product_id": "63629-1988_ff1cd958-1b7d-422c-bdfd-0fad7d98d6bc", "dosage_form": "TABLET, COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "63629-1988", "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": "225 mg/1"}], "application_number": "ANDA076550", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}