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    NDC 00781-8974-01 Desipramine Hydrochloride 75 mg/1 Details

    Desipramine Hydrochloride 75 mg/1

    Desipramine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sandoz Inc. The primary component is DESIPRAMINE HYDROCHLORIDE.

    Product Information

    NDC 00781-8974
    Product ID 0781-8974_b04d3bbb-6154-41f7-bc95-318ae2e9a800
    Associated GPIs 58200030100320
    GCN Sequence Number 046108
    GCN Sequence Number Description desipramine HCl TABLET 75 MG ORAL
    HIC3 H2U
    HIC3 Description TRICYCLIC ANTIDEPRESSANTS,REL.NON-SEL.REUPT-INHIB
    GCN 16588
    HICL Sequence Number 001645
    HICL Sequence Number Description DESIPRAMINE HCL
    Brand/Generic Generic
    Proprietary Name Desipramine Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Desipramine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 75
    Active Ingredient Units mg/1
    Substance Name DESIPRAMINE HYDROCHLORIDE
    Labeler Name Sandoz Inc
    Pharmaceutical Class Tricyclic Antidepressant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA072102
    Listing Certified Through n/a

    Package

    NDC 00781-8974-01 (00781897401)

    NDC Package Code 0781-8974-01
    Billing NDC 00781897401
    Package 100 TABLET, FILM COATED in 1 BOTTLE (0781-8974-01)
    Marketing Start Date 2018-06-27
    NDC Exclude Flag N
    Pricing Information N/A