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United States · US · US:25021-207_f327fef8-8ebd-45a2-a339-72e702c4f8b5
doxorubicin hydrochloride
Orange BookUNIISPLATC L01DB01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSagent Pharmaceuticals
CountryUS (United States)
ATC codeL01DB01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1125021207251 VIAL in 1 CARTON (25021-207-25) / 25 mL in 1 VIAL
- ndc1125021207511 VIAL in 1 CARTON (25021-207-51) / 100 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
82F2G7BL4E
DOXORUBICIN HYDROCHLORIDE
RxCUI 142433
Orange Book
A209825
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "82F2G7BL4E",
"rxcui": "142433",
"inchikey": "MWWSFMDVAYGXBV-RUELKSSGSA-N",
"display_name": "DOXORUBICIN HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"f6508535-e7a7-4e50-8d0c-43deda8d0d08": {
"match": "brand_token",
"title": "DOXORUBICIN HYDROCHLORIDE INJECTABLE, LIPOSOMAL [BLUEPOINT LABORATORIES]",
"spl_version": "5",
"published_date": "2026-05-25"
}
},
"productid": "25021-207_f327fef8-8ebd-45a2-a339-72e702c4f8b5",
"productndc": "25021-207",
"dosage_form": "INJECTION, SOLUTION",
"orange_book": {
"appl_no": "209825",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "2MG/ML",
"product_no": "001",
"approval_date": "Aug 11, 2017"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DOXORUBICIN HYDROCHLORIDE",
"proprietary_name": "doxorubicin hydrochloride",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA209825",
"marketing_category": "ANDA",
"nonproprietary_name": "doxorubicin hydrochloride",
"start_marketing_date": "20131031",
"active_numerator_strength": "2"
}Related drugs
Other records sharing ATC code L01DB01.
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