deferiprone

Generic: deferiprone

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name deferiprone
Generic Name deferiprone
Labeler hikma pharmaceuticals usa inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

deferiprone 1000 mg/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0054-0711
Product ID 0054-0711_db72caee-70a3-4561-b855-08b4c9f4a0e0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213239
Listing Expiration 2026-12-31
Marketing Start 2022-02-08

Pharmacologic Class

Established (EPC)
iron chelator [epc]
Mechanism of Action
iron chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00540711
Hyphenated Format 0054-0711

Supplemental Identifiers

RxCUI
2180997
UPC
0300540711191
UNII
2BTY8KH53L
NUI
N0000000144 N0000175522

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name deferiprone (source: ndc)
Generic Name deferiprone (source: ndc)
Application Number ANDA213239 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 50 TABLET, COATED in 1 BOTTLE (0054-0711-19)
  • 150 TABLET, COATED in 1 BOTTLE (0054-0711-23)
  • 300 TABLET, COATED in 1 BOTTLE (0054-0711-28)
source: ndc

Packages (3)

0054-0711-19 50 TABLET, COATED in 1 BOTTLE (0054-0711-19) 0054-0711-23 150 TABLET, COATED in 1 BOTTLE (0054-0711-23) 0054-0711-28 300 TABLET, COATED in 1 BOTTLE (0054-0711-28)

Ingredients (1)

deferiprone (1000 mg/1)

Linked Drug Pages (1)

Deferiprone ndc-match (0.9)

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"}