ferriprox

Generic: deferiprone

Labeler: chiesi usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name ferriprox
Generic Name deferiprone
Labeler chiesi usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

deferiprone 1000 mg/1

Manufacturer
Chiesi USA, Inc.

Identifiers & Regulatory

Product NDC 10122-103
Product ID 10122-103_f6d7984f-011e-4a3f-bcf5-6a5b2b6ef2f9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021825
Listing Expiration 2027-12-31
Marketing Start 2019-08-01

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 10122103
Hyphenated Format 10122-103

Supplemental Identifiers

RxCUI
389242 1190357 2180997 2180999 2685014 2685015
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 ferriprox (source: ndc)
Generic Name deferiprone (source: ndc)
Application Number NDA021825 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10122-103-05)
source: ndc

Packages (1)

10122-103-05 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10122-103-05)

Ingredients (1)

deferiprone (1000 mg/1)

Linked Drug Pages (1)

FERRIPROX ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f6d7984f-011e-4a3f-bcf5-6a5b2b6ef2f9", "openfda": {"nui": ["N0000000144", "N0000175522"], "unii": ["2BTY8KH53L"], "rxcui": ["389242", "1190357", "2180997", "2180999", "2685014", "2685015"], "spl_set_id": ["946718ff-df43-1baa-74d1-e5bcfbe8ad86"], "pharm_class_epc": ["Iron Chelator [EPC]"], "pharm_class_moa": ["Iron Chelating Activity [MoA]"], "manufacturer_name": ["Chiesi USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10122-103-05)", "package_ndc": "10122-103-05", "marketing_start_date": "20190801"}], "brand_name": "FERRIPROX", "product_id": "10122-103_f6d7984f-011e-4a3f-bcf5-6a5b2b6ef2f9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Iron Chelating Activity [MoA]", "Iron Chelator [EPC]"], "product_ndc": "10122-103", "generic_name": "DEFERIPRONE", "labeler_name": "Chiesi USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FERRIPROX", "active_ingredients": [{"name": "DEFERIPRONE", "strength": "1000 mg/1"}], "application_number": "NDA021825", "marketing_category": "NDA", "marketing_start_date": "20190801", "listing_expiration_date": "20271231"}