ferriprox
Generic: deferiprone
Labeler: chiesi usa, inc.Drug Facts
Product Profile
Brand Name
ferriprox
Generic Name
deferiprone
Labeler
chiesi usa, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
deferiprone 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
10122-101
Product ID
10122-101_3ec2a1ae-4ca9-43b3-a3e2-2b79c2a34172
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA208030
Listing Expiration
2026-12-31
Marketing Start
2015-09-09
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
10122101
Hyphenated Format
10122-101
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
NDA208030 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
Packaging
- 500 mL in 1 BOTTLE, PLASTIC (10122-101-50)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ec2a1ae-4ca9-43b3-a3e2-2b79c2a34172", "openfda": {"nui": ["N0000000144", "N0000175522"], "unii": ["2BTY8KH53L"], "rxcui": ["1716264", "1716268"], "spl_set_id": ["f057cf4d-b06f-4fbd-aa2e-68c5e4d8a846"], "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": "500 mL in 1 BOTTLE, PLASTIC (10122-101-50)", "package_ndc": "10122-101-50", "marketing_start_date": "20210101"}], "brand_name": "FERRIPROX", "product_id": "10122-101_3ec2a1ae-4ca9-43b3-a3e2-2b79c2a34172", "dosage_form": "SOLUTION", "pharm_class": ["Iron Chelating Activity [MoA]", "Iron Chelator [EPC]"], "product_ndc": "10122-101", "generic_name": "deferiprone", "labeler_name": "Chiesi USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FERRIPROX", "active_ingredients": [{"name": "DEFERIPRONE", "strength": "100 mg/mL"}], "application_number": "NDA208030", "marketing_category": "NDA", "marketing_start_date": "20150909", "listing_expiration_date": "20261231"}