Package 0054-0711-28

Brand: deferiprone

Generic: deferiprone
NDC Package

Package Facts

Identity

Package NDC 0054-0711-28
Digits Only 0054071128
Product NDC 0054-0711
Description

300 TABLET, COATED in 1 BOTTLE (0054-0711-28)

Marketing

Marketing Status
Marketed Since 2022-02-08
Brand deferiprone
Generic deferiprone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "db72caee-70a3-4561-b855-08b4c9f4a0e0", "openfda": {"nui": ["N0000000144", "N0000175522"], "upc": ["0300540711191"], "unii": ["2BTY8KH53L"], "rxcui": ["2180997"], "spl_set_id": ["c4f9e9be-39e7-4940-9cb0-f17772d7e524"], "pharm_class_epc": ["Iron Chelator [EPC]"], "pharm_class_moa": ["Iron Chelating Activity [MoA]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, COATED in 1 BOTTLE (0054-0711-19)", "package_ndc": "0054-0711-19", "marketing_start_date": "20220208"}, {"sample": false, "description": "150 TABLET, COATED in 1 BOTTLE (0054-0711-23)", "package_ndc": "0054-0711-23", "marketing_start_date": "20220208"}, {"sample": false, "description": "300 TABLET, COATED in 1 BOTTLE (0054-0711-28)", "package_ndc": "0054-0711-28", "marketing_start_date": "20220208"}], "brand_name": "Deferiprone", "product_id": "0054-0711_db72caee-70a3-4561-b855-08b4c9f4a0e0", "dosage_form": "TABLET, COATED", "pharm_class": ["Iron Chelating Activity [MoA]", "Iron Chelator [EPC]"], "product_ndc": "0054-0711", "generic_name": "Deferiprone", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Deferiprone", "active_ingredients": [{"name": "DEFERIPRONE", "strength": "1000 mg/1"}], "application_number": "ANDA213239", "marketing_category": "ANDA", "marketing_start_date": "20220208", "listing_expiration_date": "20261231"}