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    NDC 59651-0021-90 Dutasteride 0.5 mg/1 Details

    Dutasteride 0.5 mg/1

    Dutasteride is a ORAL CAPSULE, LIQUID FILLED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is DUTASTERIDE.

    Product Information

    NDC 59651-0021
    Product ID 59651-021_b32611f3-50ec-45bb-a671-ea10cec7829d
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Dutasteride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Dutasteride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE, LIQUID FILLED
    Route ORAL
    Active Ingredient Strength 0.5
    Active Ingredient Units mg/1
    Substance Name DUTASTERIDE
    Labeler Name Aurobindo Pharma Limited
    Pharmaceutical Class 5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202660
    Listing Certified Through 2024-12-31

    Package

    NDC 59651-0021-90 (59651002190)

    NDC Package Code 59651-021-90
    Billing NDC 59651002190
    Package 90 CAPSULE, LIQUID FILLED in 1 BOTTLE (59651-021-90)
    Marketing Start Date 2023-01-20
    NDC Exclude Flag N
    Pricing Information N/A
    << 59651-0021-30 59651-0025-01 >>

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