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    NDC 16571-0821-51 TEMOZOLOMIDE 250 mg/1 Details

    TEMOZOLOMIDE 250 mg/1

    TEMOZOLOMIDE is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Rising Pharma Holdings, Inc.. The primary component is TEMOZOLOMIDE.

    Product Information

    NDC 16571-0821
    Product ID 16571-821_f7c1aa83-a94a-4f97-bc30-66b8a89783b9
    Associated GPIs
    GCN Sequence Number 043013
    GCN Sequence Number Description temozolomide CAPSULE 250 MG ORAL
    HIC3 V1A
    HIC3 Description ANTINEOPLASTIC - ALKYLATING AGENTS
    GCN 92933
    HICL Sequence Number 020355
    HICL Sequence Number Description TEMOZOLOMIDE
    Brand/Generic Generic
    Proprietary Name TEMOZOLOMIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name temozolomide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 250
    Active Ingredient Units mg/1
    Substance Name TEMOZOLOMIDE
    Labeler Name Rising Pharma Holdings, Inc.
    Pharmaceutical Class Alkylating Activity [MoA], Alkylating Drug [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA206309
    Listing Certified Through 2024-12-31

    Package

    NDC 16571-0821-51 (16571082151)

    NDC Package Code 16571-821-51
    Billing NDC 16571082151
    Package 5 CAPSULE in 1 BOTTLE (16571-821-51)
    Marketing Start Date 2022-10-04
    NDC Exclude Flag N
    Pricing Information N/A