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
Routes
ORAL
Active Ingredients

deferiprone 1000 mg/1

Manufacturer
Chiesi USA, Inc.

Identifiers & Regulatory

Product NDC 10122-104
Product ID 10122-104_f6d7984f-011e-4a3f-bcf5-6a5b2b6ef2f9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA212269
Listing Expiration 2027-12-31
Marketing Start 2020-05-19

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 10122104
Hyphenated Format 10122-104

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 NDA212269 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 50 TABLET in 1 BLISTER PACK (10122-104-01)
  • 50 TABLET in 1 BOTTLE, PLASTIC (10122-104-05)
source: ndc

Packages (2)

10122-104-01 50 TABLET in 1 BLISTER PACK (10122-104-01) 10122-104-05 50 TABLET in 1 BOTTLE, PLASTIC (10122-104-05)

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 in 1 BLISTER PACK (10122-104-01)", "package_ndc": "10122-104-01", "marketing_start_date": "20200519"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (10122-104-05)", "package_ndc": "10122-104-05", "marketing_start_date": "20211201"}], "brand_name": "FERRIPROX", "product_id": "10122-104_f6d7984f-011e-4a3f-bcf5-6a5b2b6ef2f9", "dosage_form": "TABLET", "pharm_class": ["Iron Chelating Activity [MoA]", "Iron Chelator [EPC]"], "product_ndc": "10122-104", "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": "NDA212269", "marketing_category": "NDA", "marketing_start_date": "20200519", "listing_expiration_date": "20271231"}