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    NDC 70518-2177-01 Prazosin Hydrochloride 1 mg/1 Details

    Prazosin Hydrochloride 1 mg/1

    Prazosin Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is PRAZOSIN HYDROCHLORIDE.

    Product Information

    NDC 70518-2177
    Product ID 70518-2177_fea9548e-72b9-277a-e053-6394a90add93
    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 Prazosin Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Prazosin Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 1
    Active Ingredient Units mg/1
    Substance Name PRAZOSIN HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA210971
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2177-01 (70518217701)

    NDC Package Code 70518-2177-1
    Billing NDC 70518217701
    Package 30 CAPSULE in 1 BLISTER PACK (70518-2177-1)
    Marketing Start Date 2020-05-28
    NDC Exclude Flag N
    Pricing Information N/A