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    NDC 53002-1663-00 Tamsulosin Hydrochloride 0.4 mg/1 Details

    Tamsulosin Hydrochloride 0.4 mg/1

    Tamsulosin Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by RPK Pharmaceuticals, Inc.. The primary component is TAMSULOSIN HYDROCHLORIDE.

    Product Information

    NDC 53002-1663
    Product ID 53002-1663_eec67425-e83e-4ff3-8722-e852f5a219b6
    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 Tamsulosin Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Tamsulosin Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 0.4
    Active Ingredient Units mg/1
    Substance Name TAMSULOSIN HYDROCHLORIDE
    Labeler Name RPK Pharmaceuticals, Inc.
    Pharmaceutical Class Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202433
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-1663-00 (53002166300)

    NDC Package Code 53002-1663-0
    Billing NDC 53002166300
    Package 100 CAPSULE in 1 BOTTLE (53002-1663-0)
    Marketing Start Date 2023-01-01
    NDC Exclude Flag N
    Pricing Information N/A