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    NDC 68788-7824-01 Prazosin Hydrochloride 5 mg/1 Details

    Prazosin Hydrochloride 5 mg/1

    Prazosin Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by P)referred Pharmaceuticals Inc.. The primary component is PRAZOSIN HYDROCHLORIDE.

    Product Information

    NDC 68788-7824
    Product ID 68788-7824_7111161f-3a9c-4c64-80a9-80f419f4dcbe
    Associated GPIs 36202030100115
    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 5
    Active Ingredient Units mg/1
    Substance Name PRAZOSIN HYDROCHLORIDE
    Labeler Name P)referred Pharmaceuticals Inc.
    Pharmaceutical Class Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA071745
    Listing Certified Through 2023-12-31

    Package

    NDC 68788-7824-01 (68788782401)

    NDC Package Code 68788-7824-1
    Billing NDC 68788782401
    Package 100 CAPSULE in 1 BOTTLE (68788-7824-1)
    Marketing Start Date 2021-01-05
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL fb8ccfc7-4eae-4f7b-bb73-b46d7d6e6a06 Details

    Revised: 9/2022