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    NDC 70518-3017-00 DOXEPIN HYDROCHLORIDE 50 mg/1 Details

    DOXEPIN HYDROCHLORIDE 50 mg/1

    DOXEPIN HYDROCHLORIDE is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is DOXEPIN HYDROCHLORIDE.

    Product Information

    NDC 70518-3017
    Product ID 70518-3017_05438006-8a12-8c47-e063-6394a90a4bc1
    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 50
    Active Ingredient Units mg/1
    Substance Name DOXEPIN HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Tricyclic Antidepressant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA213063
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3017-00 (70518301700)

    NDC Package Code 70518-3017-0
    Billing NDC 70518301700
    Package 30 CAPSULE in 1 BLISTER PACK (70518-3017-0)
    Marketing Start Date 2021-02-05
    NDC Exclude Flag N
    Pricing Information N/A