Search by Drug Name or NDC

    NDC 68788-7050-01 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 Preferred Pharmaceuticals, Inc.. The primary component is TAMSULOSIN HYDROCHLORIDE.

    Product Information

    NDC 68788-7050
    Product ID 68788-7050_d2f7abf7-662b-4760-8edb-6e99fa170f47
    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 Preferred 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 68788-7050-01 (68788705001)

    NDC Package Code 68788-7050-1
    Billing NDC 68788705001
    Package 100 CAPSULE in 1 BOTTLE (68788-7050-1)
    Marketing Start Date 2020-06-01
    NDC Exclude Flag N
    Pricing Information N/A