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United States · US · US:31722-029_17f07dc1-8041-d263-e063-6394a90ae223
DEFERASIROX
Orange BookUNIISPLATC V03AC03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCamber Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeV03AC03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11317220293230 PACKET in 1 CARTON (31722-029-32) / 1 GRANULE in 1 PACKET
Annotations
UNII (FDA Substance ID)
V8G4MOF2V9
DEFERASIROX
RxCUI 614373
Orange Book
A216229
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "V8G4MOF2V9",
"rxcui": "614373",
"inchikey": "BOFQWVMAQOTZIW-UHFFFAOYSA-N",
"display_name": "DEFERASIROX",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"a03c7657-fdca-4acb-ad82-c24680e90eae": {
"match": "brand_token",
"title": "DEFERASIROX TABLET, FOR SUSPENSION [NOVADOZ PHARMACEUTICALS LLC]",
"spl_version": "1",
"published_date": "2026-01-30"
}
},
"productid": "31722-029_17f07dc1-8041-d263-e063-6394a90ae223",
"productndc": "31722-029",
"dosage_form": "GRANULE",
"orange_book": {
"appl_no": "216229",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "180MG",
"product_no": "001",
"approval_date": "Sep 22, 2022"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "360MG",
"product_no": "002",
"approval_date": "Sep 22, 2022"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "90MG",
"product_no": "003",
"approval_date": "Mar 16, 2023"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DEFERASIROX",
"proprietary_name": "DEFERASIROX",
"active_ingred_unit": "mg/1",
"application_number": "ANDA216229",
"marketing_category": "ANDA",
"nonproprietary_name": "DEFERASIROX",
"start_marketing_date": "20230316",
"active_numerator_strength": "90"
}Related drugs
Other records sharing ATC code V03AC03.
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