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    NDC 71335-1021-01 DESIPRAMINE HYDROCHLORIDE 10 mg/1 Details

    DESIPRAMINE HYDROCHLORIDE 10 mg/1

    DESIPRAMINE HYDROCHLORIDE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is DESIPRAMINE HYDROCHLORIDE.

    Product Information

    NDC 71335-1021
    Product ID 71335-1021_9c8f89b0-5da1-42ca-a3dd-b81f6d4e7a73
    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 DESIPRAMINE HYDROCHLORIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name desipramine hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name DESIPRAMINE HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Tricyclic Antidepressant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207433
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-1021-01 (71335102101)

    NDC Package Code 71335-1021-1
    Billing NDC 71335102101
    Package 30 TABLET in 1 BOTTLE (71335-1021-1)
    Marketing Start Date 2018-11-06
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 9c8f89b0-5da1-42ca-a3dd-b81f6d4e7a73 Details

    Revised: 12/2021