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United States · US · US:82293-022_2007980f-ffca-6d8f-e063-6294a90ae3ff
pazopanib
Orange BookUNIISPLATC L01EX03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNovugen Pharma (USA) LLC.
CountryUS (United States)
ATC codeL01EX03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc118229302210120 TABLET, FILM COATED in 1 BOTTLE (82293-022-10)
Annotations
UNII (FDA Substance ID)
33Y9ANM545
PAZOPANIB HYDROCHLORIDE
RxCUI 732187
Orange Book
A218231
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "33Y9ANM545",
"rxcui": "732187",
"inchikey": "MQHIQUBXFFAOMK-UHFFFAOYSA-N",
"display_name": "PAZOPANIB HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"d3e8dd09-d7d2-43da-8f63-bdf0ea0fcdf5": {
"match": "brand_token",
"title": "PAZOPANIB TABLET, FILM COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.]",
"spl_version": "4",
"published_date": "2026-05-28"
}
},
"productid": "82293-022_2007980f-ffca-6d8f-e063-6294a90ae3ff",
"productndc": "82293-022",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "218231",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 200MG BASE",
"product_no": "001",
"approval_date": "Apr 23, 2024"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PAZOPANIB HYDROCHLORIDE",
"proprietary_name": "pazopanib",
"active_ingred_unit": "mg/1",
"application_number": "ANDA218231",
"marketing_category": "ANDA",
"nonproprietary_name": "pazopanib hydrochloride",
"start_marketing_date": "20240424",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code L01EX03.
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