Lenalidomide

Orange BookUNIISPLATC L04AX04

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerAurobindo Pharma Limited

CountryUS (United States)

ATC codeL04AX04

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
5965134301
100 CAPSULE in 1 BOTTLE (59651-343-01)
ndc11
5965134307
1 BLISTER PACK in 1 CARTON (59651-343-07) / 7 CAPSULE in 1 BLISTER PACK
ndc11
5965134328
28 CAPSULE in 1 BOTTLE (59651-343-28)

Annotations

UNII (FDA Substance ID)

F0P408N6V4

LENALIDOMIDE

RxCUI 342369

Orange Book

A213885

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": "59651-343_f022fe20-76ac-4825-8986-6e1ec95b0b21",
  "productndc": "59651-343",
  "dosage_form": "CAPSULE",
  "orange_book": {
    "appl_no": "213885",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2.5MG",
        "product_no": "001",
        "approval_date": "Mar 6, 2023"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "002",
        "approval_date": "Mar 6, 2023"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "003",
        "approval_date": "Mar 6, 2023"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "15MG",
        "product_no": "004",
        "approval_date": "Mar 6, 2023"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "005",
        "approval_date": "Mar 6, 2023"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "006",
        "approval_date": "Mar 6, 2023"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LENALIDOMIDE",
  "proprietary_name": "Lenalidomide",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA213885",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Lenalidomide",
  "start_marketing_date": "20230306",
  "active_numerator_strength": "5"
}

Related drugs

Other records sharing ATC code L04AX04.

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