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    NDC 63304-0046-22 Lenalidomide 25 mg/1 Details

    Lenalidomide 25 mg/1

    Lenalidomide is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is LENALIDOMIDE.

    Product Information

    NDC 63304-0046
    Product ID 63304-046_3b4a2db3-5368-400c-81f6-ffa0b7a34653
    Associated GPIs
    GCN Sequence Number 061114
    GCN Sequence Number Description lenalidomide CAPSULE 25 MG ORAL
    HIC3 V1M
    HIC3 Description ANTINEOPLASTIC IMMUNOMODULATOR AGENTS
    GCN 27277
    HICL Sequence Number 033412
    HICL Sequence Number Description LENALIDOMIDE
    Brand/Generic Generic
    Proprietary Name Lenalidomide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Lenalidomide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name LENALIDOMIDE
    Labeler Name Sun Pharmaceutical Industries, Inc.
    Pharmaceutical Class Thalidomide Analog [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA211846
    Listing Certified Through 2024-12-31

    Package

    NDC 63304-0046-22 (63304004622)

    NDC Package Code 63304-046-22
    Billing NDC 63304004622
    Package 21 CAPSULE in 1 BOTTLE (63304-046-22)
    Marketing Start Date 2023-03-04
    NDC Exclude Flag N
    Pricing Information N/A