deferiprone

Generic: deferiprone

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name deferiprone
Generic Name deferiprone
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

deferiprone 1000 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-4237
Product ID 51672-4237_3631d351-4653-3512-e063-6394a90a81c0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208800
Listing Expiration 2026-12-31
Marketing Start 2024-02-05

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 516724237
Hyphenated Format 51672-4237

Supplemental Identifiers

RxCUI
389242 2180997
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 ANDA208800 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 50 TABLET in 1 BOTTLE (51672-4237-4)
source: ndc

Packages (1)

51672-4237-4 50 TABLET in 1 BOTTLE (51672-4237-4)

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": "3631d351-4653-3512-e063-6394a90a81c0", "openfda": {"nui": ["N0000000144", "N0000175522"], "unii": ["2BTY8KH53L"], "rxcui": ["389242", "2180997"], "spl_set_id": ["5af1643d-4c6e-4668-ae9b-1046f0ad6d8a"], "pharm_class_epc": ["Iron Chelator [EPC]"], "pharm_class_moa": ["Iron Chelating Activity [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (51672-4237-4)", "package_ndc": "51672-4237-4", "marketing_start_date": "20240205"}], "brand_name": "Deferiprone", "product_id": "51672-4237_3631d351-4653-3512-e063-6394a90a81c0", "dosage_form": "TABLET", "pharm_class": ["Iron Chelating Activity [MoA]", "Iron Chelator [EPC]"], "product_ndc": "51672-4237", "generic_name": "Deferiprone", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Deferiprone", "active_ingredients": [{"name": "DEFERIPRONE", "strength": "1000 mg/1"}], "application_number": "ANDA208800", "marketing_category": "ANDA", "marketing_start_date": "20240205", "listing_expiration_date": "20261231"}