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United States · US · US:67457-436_fa646028-c150-4d9b-80a8-8add851d684d
Doxorubicin Hydrochloride
Orange BookUNIISPLATC L01DB01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMylan Institutional LLC
CountryUS (United States)
ATC codeL01DB01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1167457436501 VIAL in 1 CARTON (67457-436-50) / 25 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
82F2G7BL4E
DOXORUBICIN HYDROCHLORIDE
RxCUI 142433
Orange Book
A200170
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": "67457-436_fa646028-c150-4d9b-80a8-8add851d684d",
"productndc": "67457-436",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"orange_book": {
"appl_no": "200170",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG/VIAL",
"product_no": "001",
"approval_date": "Oct 28, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "50MG/VIAL",
"product_no": "002",
"approval_date": "Oct 28, 2011"
}
],
"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": "ANDA200170",
"marketing_category": "ANDA",
"nonproprietary_name": "Doxorubicin Hydrochloride",
"start_marketing_date": "20140227",
"active_numerator_strength": "2"
}Related drugs
Other records sharing ATC code L01DB01.
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