Package 72162-1751-1

Brand: propafenone hydrochloride

Generic: propafenone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1751-1
Digits Only 7216217511
Product NDC 72162-1751
Product ID 72162-1751_4bc2f877-9021-c8aa-e063-6294a90adc52
Description

100 TABLET, COATED in 1 BOTTLE (72162-1751-1)

Marketing

Marketing Status
Marketed Since 2023-08-30
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": "4bc2f877-9021-c8aa-e063-6294a90adc52", "openfda": {"unii": ["33XCH0HOCD"], "rxcui": ["861424"], "spl_set_id": ["680a803d-3d4d-4ca3-b1ce-7d7e3ff8a626"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (72162-1751-1)", "package_ndc": "72162-1751-1", "marketing_start_date": "20230830"}], "brand_name": "Propafenone Hydrochloride", "product_id": "72162-1751_4bc2f877-9021-c8aa-e063-6294a90adc52", "dosage_form": "TABLET, COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "72162-1751", "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": "150 mg/1"}], "application_number": "ANDA076550", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20271231"}