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United States · US · US:63304-116_522bc5e6-38ab-65fd-e063-6394a90a97d6
Pazopanib
Orange BookUNIISPLATC L01EX03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSUN PHARMACEUTICAL INDUSTRIES, INC.
CountryUS (United States)
ATC codeL01EX03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc116330411613120 TABLET, FILM COATED in 1 BOTTLE (63304-116-13)
- ndc11633041163030 TABLET, FILM COATED in 1 BOTTLE (63304-116-30)
Annotations
UNII (FDA Substance ID)
33Y9ANM545
PAZOPANIB HYDROCHLORIDE
RxCUI 732187
Orange Book
A215837
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": "63304-116_522bc5e6-38ab-65fd-e063-6394a90a97d6",
"productndc": "63304-116",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "215837",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 200MG BASE",
"product_no": "001",
"approval_date": "Oct 19, 2023"
}
],
"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": "ANDA215837",
"marketing_category": "ANDA",
"nonproprietary_name": "Pazopanib",
"start_marketing_date": "20231020",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code L01EX03.
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