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    NDC 70868-0810-10 Imipramine Hydrochloride 25 mg/1 Details

    Imipramine Hydrochloride 25 mg/1

    Imipramine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Key Therapeutics. The primary component is IMIPRAMINE HYDROCHLORIDE.

    Product Information

    NDC 70868-0810
    Product ID 70868-810_ed673cf8-bea3-4d5a-9171-3a23ffc696c3
    Associated GPIs
    GCN Sequence Number 046069
    GCN Sequence Number Description imipramine HCl TABLET 25 MG ORAL
    HIC3 H2U
    HIC3 Description TRICYCLIC ANTIDEPRESSANTS,REL.NON-SEL.REUPT-INHIB
    GCN 16542
    HICL Sequence Number 001641
    HICL Sequence Number Description IMIPRAMINE HCL
    Brand/Generic Generic
    Proprietary Name Imipramine Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Imipramine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name IMIPRAMINE HYDROCHLORIDE
    Labeler Name Key Therapeutics
    Pharmaceutical Class Tricyclic Antidepressant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA040751
    Listing Certified Through 2024-12-31

    Package

    NDC 70868-0810-10 (70868081010)

    NDC Package Code 70868-810-10
    Billing NDC 70868081010
    Package 100 TABLET, FILM COATED in 1 BOTTLE (70868-810-10)
    Marketing Start Date 2022-07-18
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 9c685c94-64cd-442a-ade7-193c62d7a058 Details

    Revised: 7/2022