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United States · US · US:43598-512_023f2dc9-b878-9d13-44d0-894310c6b8da
Lenalidomide
Orange BookUNIISPLATC L04AX04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDr. Reddy's Laboratories Inc.
CountryUS (United States)
ATC codeL04AX04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc114359851201100 CAPSULE in 1 BOTTLE (43598-512-01)
- ndc11435985126328 CAPSULE in 1 BOTTLE (43598-512-63)
Annotations
UNII (FDA Substance ID)
F0P408N6V4
LENALIDOMIDE
RxCUI 342369
Orange Book
A209348
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": "43598-512_023f2dc9-b878-9d13-44d0-894310c6b8da",
"productndc": "43598-512",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "209348",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "2.5MG",
"product_no": "001",
"approval_date": "Oct 14, 2021"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "20MG",
"product_no": "002",
"approval_date": "Oct 14, 2021"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "003",
"approval_date": "Aug 30, 2022"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "10MG",
"product_no": "004",
"approval_date": "Aug 30, 2022"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "15MG",
"product_no": "005",
"approval_date": "Aug 30, 2022"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "006",
"approval_date": "Aug 30, 2022"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LENALIDOMIDE",
"proprietary_name": "Lenalidomide",
"active_ingred_unit": "mg/1",
"application_number": "ANDA209348",
"marketing_category": "ANDA",
"nonproprietary_name": "Lenalidomide",
"start_marketing_date": "20220907",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code L04AX04.
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