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    NDC 57664-0053-72 Trazodone Hydrochloride 150 mg/1 Details

    Trazodone Hydrochloride 150 mg/1

    Trazodone Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is TRAZODONE HYDROCHLORIDE.

    Product Information

    NDC 57664-0053
    Product ID 57664-053_f291a9f6-4b36-753c-e053-2a95a90a181a
    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 Trazodone Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Trazodone Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 150
    Active Ingredient Units mg/1
    Substance Name TRAZODONE HYDROCHLORIDE
    Labeler Name Sun Pharmaceutical Industries, Inc.
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA073137
    Listing Certified Through 2024-12-31

    Package

    NDC 57664-0053-72 (57664005372)

    NDC Package Code 57664-053-72
    Billing NDC 57664005372
    Package 100 TABLET in 1 BOTTLE, PLASTIC (57664-053-72)
    Marketing Start Date 2022-10-03
    NDC Exclude Flag N
    Pricing Information N/A
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