Package 72162-1753-1
Brand: propafenone hydrochloride
Generic: propafenone hydrochloridePackage Facts
Identity
Package NDC
72162-1753-1
Digits Only
7216217531
Product NDC
72162-1753
Description
100 TABLET, COATED in 1 BOTTLE (72162-1753-1)
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": "4bc381ad-9816-bf1a-e063-6394a90a0f6d", "openfda": {"unii": ["33XCH0HOCD"], "rxcui": ["861430"], "spl_set_id": ["739b7624-952d-4343-b720-974d30e284d9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (72162-1753-1)", "package_ndc": "72162-1753-1", "marketing_start_date": "20230913"}], "brand_name": "Propafenone Hydrochloride", "product_id": "72162-1753_4bc381ad-9816-bf1a-e063-6394a90a0f6d", "dosage_form": "TABLET, COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "72162-1753", "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": "20271231"}