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United States · US · US:70748-339_e9f76142-15d0-4234-8f2e-5f5014160eff
DOXORUBICIN HYDROCHLORIDE
Orange BookUNIISPLATC L01DB01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLupin Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeL01DB01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1170748339011 VIAL, SINGLE-USE in 1 CARTON (70748-339-01) / 10 mL in 1 VIAL, SINGLE-USE
Annotations
UNII (FDA Substance ID)
82F2G7BL4E
DOXORUBICIN HYDROCHLORIDE
RxCUI 142433
Orange Book
A215178
ABAB
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": "70748-339_e9f76142-15d0-4234-8f2e-5f5014160eff",
"productndc": "70748-339",
"dosage_form": "INJECTION, SUSPENSION, LIPOSOMAL",
"orange_book": {
"appl_no": "215178",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "20MG/10ML (2MG/ML)",
"product_no": "001",
"approval_date": "Jul 16, 2024"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "50MG/25ML (2MG/ML)",
"product_no": "002",
"approval_date": "Jul 16, 2024"
}
],
"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": "ANDA215178",
"marketing_category": "ANDA",
"nonproprietary_name": "DOXORUBICIN HYDROCHLORIDE",
"start_marketing_date": "20240826",
"active_numerator_strength": "2"
}Related drugs
Other records sharing ATC code L01DB01.
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