Package 63629-1981-1

Brand: flecainide acetate

Generic: flecainide acetate tablet
NDC Package

Package Facts

Identity

Package NDC 63629-1981-1
Digits Only 6362919811
Product NDC 63629-1981
Description

100 TABLET in 1 BOTTLE (63629-1981-1)

Marketing

Marketing Status
Marketed Since 2021-01-15
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": "f2b5a016-df67-45ce-933e-b1f39c8aa6d0", "openfda": {"unii": ["M8U465Q1WQ"], "rxcui": ["886671"], "spl_set_id": ["2028149f-6fc0-455c-bac5-729eeaa4aee5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1981-1)", "package_ndc": "63629-1981-1", "marketing_start_date": "20210115"}], "brand_name": "Flecainide Acetate", "product_id": "63629-1981_f2b5a016-df67-45ce-933e-b1f39c8aa6d0", "dosage_form": "TABLET", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "63629-1981", "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": "150 mg/1"}], "application_number": "ANDA075882", "marketing_category": "ANDA", "marketing_start_date": "20151228", "listing_expiration_date": "20261231"}