Package 72162-1760-1

Brand: flecainide acetate

Generic: flecainide acetate tablet
NDC Package

Package Facts

Identity

Package NDC 72162-1760-1
Digits Only 7216217601
Product NDC 72162-1760
Description

100 TABLET in 1 BOTTLE (72162-1760-1)

Marketing

Marketing Status
Marketed Since 2023-08-30
Brand flecainide acetate
Generic flecainide acetate tablet
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d3d69961-0cb7-4439-acdf-99bec2148aac", "openfda": {"unii": ["M8U465Q1WQ"], "rxcui": ["886662"], "spl_set_id": ["d34fae51-3658-4456-b3ea-1217f0f52260"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1760-1)", "package_ndc": "72162-1760-1", "marketing_start_date": "20230830"}], "brand_name": "Flecainide Acetate", "product_id": "72162-1760_d3d69961-0cb7-4439-acdf-99bec2148aac", "dosage_form": "TABLET", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "72162-1760", "generic_name": "Flecainide Acetate Tablet", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Flecainide Acetate", "active_ingredients": [{"name": "FLECAINIDE ACETATE", "strength": "50 mg/1"}], "application_number": "ANDA075882", "marketing_category": "ANDA", "marketing_start_date": "20151228", "listing_expiration_date": "20261231"}