deferiprone

Generic: deferiprone

Labeler: dr. reddy's laboratories, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name deferiprone
Generic Name deferiprone
Labeler dr. reddy's laboratories, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

deferiprone 500 mg/1

Manufacturer
DR. REDDY'S LABORATORIES, INC.

Identifiers & Regulatory

Product NDC 75907-349
Product ID 75907-349_c3247274-c72a-4181-9638-58f7ff14729c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA220132
Listing Expiration 2026-12-31
Marketing Start 2025-12-15

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 75907349
Hyphenated Format 75907-349

Supplemental Identifiers

RxCUI
389242 2180997
UPC
0375907349010 0375907348501
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 ANDA220132 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, COATED in 1 BOTTLE (75907-349-01)
source: ndc

Packages (1)

75907-349-01 100 TABLET, COATED in 1 BOTTLE (75907-349-01)

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": "c3247274-c72a-4181-9638-58f7ff14729c", "openfda": {"nui": ["N0000000144", "N0000175522"], "upc": ["0375907349010", "0375907348501"], "unii": ["2BTY8KH53L"], "rxcui": ["389242", "2180997"], "spl_set_id": ["67139215-1154-4e1a-ae15-0f3cd8af5177"], "pharm_class_epc": ["Iron Chelator [EPC]"], "pharm_class_moa": ["Iron Chelating Activity [MoA]"], "manufacturer_name": ["DR. REDDY'S LABORATORIES, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (75907-349-01)", "package_ndc": "75907-349-01", "marketing_start_date": "20251215"}], "brand_name": "DEFERIPRONE", "product_id": "75907-349_c3247274-c72a-4181-9638-58f7ff14729c", "dosage_form": "TABLET, COATED", "pharm_class": ["Iron Chelating Activity [MoA]", "Iron Chelator [EPC]"], "product_ndc": "75907-349", "generic_name": "deferiprone", "labeler_name": "DR. REDDY'S LABORATORIES, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEFERIPRONE", "active_ingredients": [{"name": "DEFERIPRONE", "strength": "500 mg/1"}], "application_number": "ANDA220132", "marketing_category": "ANDA", "marketing_start_date": "20251215", "listing_expiration_date": "20261231"}