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United States · US · US:70377-051_709e3342-23d5-10cd-3241-5ef6fdf924fe
Lenalidomide
Orange BookUNIISPLATC L04AX04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBIOCON PHARMA INC.,
CountryUS (United States)
ATC codeL04AX04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc117037705112100 CAPSULE in 1 BOTTLE (70377-051-12)
- ndc11703770511328 CAPSULE in 1 BOTTLE (70377-051-13)
Annotations
UNII (FDA Substance ID)
F0P408N6V4
LENALIDOMIDE
RxCUI 342369
Orange Book
A215759
ABABABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "F0P408N6V4",
"rxcui": "342369",
"inchikey": "GOTYRUGSSMKFNF-UHFFFAOYSA-N",
"display_name": "LENALIDOMIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"da7b5dda-79ed-4c4a-88aa-52394fdc7c54": {
"match": "brand_token",
"title": "LENALIDOMIDE CAPSULE [AMNEAL PHARMACEUTICALS NY LLC]",
"spl_version": "6",
"published_date": "2026-05-20"
}
},
"productid": "70377-051_709e3342-23d5-10cd-3241-5ef6fdf924fe",
"productndc": "70377-051",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "215759",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "2.5MG",
"product_no": "001",
"approval_date": "Mar 3, 2025"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "002",
"approval_date": "Mar 3, 2025"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "10MG",
"product_no": "003",
"approval_date": "Mar 3, 2025"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "15MG",
"product_no": "004",
"approval_date": "Mar 3, 2025"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "20MG",
"product_no": "005",
"approval_date": "Mar 3, 2025"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "006",
"approval_date": "Mar 3, 2025"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LENALIDOMIDE",
"proprietary_name": "Lenalidomide",
"active_ingred_unit": "mg/1",
"application_number": "ANDA215759",
"marketing_category": "ANDA",
"nonproprietary_name": "Lenalidomide",
"start_marketing_date": "20250303",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code L04AX04.
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