Package 62559-382-01

Brand: flecainide acetate

Generic: flecainide acetate tablet
NDC Package

Package Facts

Identity

Package NDC 62559-382-01
Digits Only 6255938201
Product NDC 62559-382
Description

100 TABLET in 1 BOTTLE (62559-382-01)

Marketing

Marketing Status
Marketed Since 2015-12-28
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": "74b708a0-2859-4efd-98a6-0c2f04d20114", "openfda": {"upc": ["0362559380010", "0362559382014", "0362559381017"], "unii": ["M8U465Q1WQ"], "rxcui": ["886662", "886666", "886671"], "spl_set_id": ["5a12889a-52ce-4dc4-9240-22d126f071ac"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62559-382-01)", "package_ndc": "62559-382-01", "marketing_start_date": "20151228"}], "brand_name": "Flecainide Acetate", "product_id": "62559-382_74b708a0-2859-4efd-98a6-0c2f04d20114", "dosage_form": "TABLET", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "62559-382", "generic_name": "Flecainide Acetate Tablet", "labeler_name": "ANI Pharmaceuticals, Inc.", "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"}