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    NDC 42806-0532-01 Doxepin Hydrochloride 75 mg/1 Details

    Doxepin Hydrochloride 75 mg/1

    Doxepin Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Epic Pharma, LLC. The primary component is DOXEPIN HYDROCHLORIDE.

    Product Information

    NDC 42806-0532
    Product ID 42806-532_baef2304-82cb-41cc-b671-51b3b7886f55
    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 Doxepin Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Doxepin Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 75
    Active Ingredient Units mg/1
    Substance Name DOXEPIN HYDROCHLORIDE
    Labeler Name Epic Pharma, LLC
    Pharmaceutical Class Tricyclic Antidepressant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA210675
    Listing Certified Through 2024-12-31

    Package

    NDC 42806-0532-01 (42806053201)

    NDC Package Code 42806-532-01
    Billing NDC 42806053201
    Package 100 CAPSULE in 1 BOTTLE (42806-532-01)
    Marketing Start Date 2022-03-03
    NDC Exclude Flag N
    Pricing Information N/A