deferasirox

Generic: deferasirox

Labeler: novadoz pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name deferasirox
Generic Name deferasirox
Labeler novadoz pharmaceuticals llc
Dosage Form TABLET, FOR SUSPENSION
Routes
ORAL
Active Ingredients

deferasirox 500 mg/1

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-391
Product ID 72205-391_a03c7657-fdca-4acb-ad82-c24680e90eae
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209878
Listing Expiration 2027-12-31
Marketing Start 2019-11-20

Pharmacologic Class

Established (EPC)
iron chelator [epc]
Mechanism of Action
iron chelating activity [moa] cytochrome p450 3a4 inducers [moa] cytochrome p450 2c8 inhibitors [moa] cytochrome p450 1a2 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72205391
Hyphenated Format 72205-391

Supplemental Identifiers

RxCUI
597768 597770 597772
UPC
0372205389014 0372205391017 0372205390010
UNII
V8G4MOF2V9
NUI
N0000000144 N0000175522 N0000185506 N0000187062 N0000182138

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 deferasirox (source: ndc)
Generic Name deferasirox (source: ndc)
Application Number ANDA209878 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 TABLET, FOR SUSPENSION in 1 BOTTLE (72205-391-01)
  • 90 TABLET, FOR SUSPENSION in 1 BOTTLE (72205-391-02)
  • 500 TABLET, FOR SUSPENSION in 1 BOTTLE (72205-391-03)
  • 10 BLISTER PACK in 1 CARTON (72205-391-05) / 10 TABLET, FOR SUSPENSION in 1 BLISTER PACK
source: ndc

Packages (4)

72205-391-01 30 TABLET, FOR SUSPENSION in 1 BOTTLE (72205-391-01) 72205-391-02 90 TABLET, FOR SUSPENSION in 1 BOTTLE (72205-391-02) 72205-391-03 500 TABLET, FOR SUSPENSION in 1 BOTTLE (72205-391-03) 72205-391-05 10 BLISTER PACK in 1 CARTON (72205-391-05) / 10 TABLET, FOR SUSPENSION in 1 BLISTER PACK

Ingredients (1)

deferasirox (500 mg/1)

Linked Drug Pages (1)

Deferasirox ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a03c7657-fdca-4acb-ad82-c24680e90eae", "openfda": {"nui": ["N0000000144", "N0000175522", "N0000185506", "N0000187062", "N0000182138"], "upc": ["0372205389014", "0372205391017", "0372205390010"], "unii": ["V8G4MOF2V9"], "rxcui": ["597768", "597770", "597772"], "spl_set_id": ["a03c7657-fdca-4acb-ad82-c24680e90eae"], "pharm_class_epc": ["Iron Chelator [EPC]"], "pharm_class_moa": ["Iron Chelating Activity [MoA]", "Cytochrome P450 3A4 Inducers [MoA]", "Cytochrome P450 2C8 Inhibitors [MoA]", "Cytochrome P450 1A2 Inhibitors [MoA]"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FOR SUSPENSION in 1 BOTTLE (72205-391-01)", "package_ndc": "72205-391-01", "marketing_start_date": "20260129"}, {"sample": false, "description": "90 TABLET, FOR SUSPENSION in 1 BOTTLE (72205-391-02)", "package_ndc": "72205-391-02", "marketing_start_date": "20260129"}, {"sample": false, "description": "500 TABLET, FOR SUSPENSION in 1 BOTTLE (72205-391-03)", "package_ndc": "72205-391-03", "marketing_start_date": "20260129"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (72205-391-05)  / 10 TABLET, FOR SUSPENSION in 1 BLISTER PACK", "package_ndc": "72205-391-05", "marketing_start_date": "20260129"}], "brand_name": "Deferasirox", "product_id": "72205-391_a03c7657-fdca-4acb-ad82-c24680e90eae", "dosage_form": "TABLET, FOR SUSPENSION", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Cytochrome P450 2C8 Inhibitors [MoA]", "Cytochrome P450 3A4 Inducers [MoA]", "Iron Chelating Activity [MoA]", "Iron Chelator [EPC]"], "product_ndc": "72205-391", "generic_name": "Deferasirox", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Deferasirox", "active_ingredients": [{"name": "DEFERASIROX", "strength": "500 mg/1"}], "application_number": "ANDA209878", "marketing_category": "ANDA", "marketing_start_date": "20191120", "listing_expiration_date": "20271231"}