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 500 mg/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0054-0576
Product ID 0054-0576_85bc2162-59ea-409a-94c2-0edef74922f5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213239
Listing Expiration 2026-12-31
Marketing Start 2021-06-03

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 00540576
Hyphenated Format 0054-0576

Supplemental Identifiers

RxCUI
389242
UPC
0300540576288 0300540576257
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
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, COATED in 1 BOTTLE (0054-0576-25)
source: ndc

Packages (1)

0054-0576-25 100 TABLET, COATED in 1 BOTTLE (0054-0576-25)

Ingredients (1)

deferiprone (500 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": "85bc2162-59ea-409a-94c2-0edef74922f5", "openfda": {"nui": ["N0000000144", "N0000175522"], "upc": ["0300540576288", "0300540576257"], "unii": ["2BTY8KH53L"], "rxcui": ["389242"], "spl_set_id": ["d7ea0a84-c328-4636-8cd6-ad75f2074b22"], "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": "100 TABLET, COATED in 1 BOTTLE (0054-0576-25)", "package_ndc": "0054-0576-25", "marketing_start_date": "20210603"}], "brand_name": "Deferiprone", "product_id": "0054-0576_85bc2162-59ea-409a-94c2-0edef74922f5", "dosage_form": "TABLET, COATED", "pharm_class": ["Iron Chelating Activity [MoA]", "Iron Chelator [EPC]"], "product_ndc": "0054-0576", "generic_name": "Deferiprone", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Deferiprone", "active_ingredients": [{"name": "DEFERIPRONE", "strength": "500 mg/1"}], "application_number": "ANDA213239", "marketing_category": "ANDA", "marketing_start_date": "20210603", "listing_expiration_date": "20261231"}