Package 72162-1753-1

Brand: propafenone hydrochloride

Generic: propafenone hydrochloride
NDC Package

Package 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
Marketed Since 2023-09-13
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"}