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    NDC 70518-2795-00 TRAMADOL HYDROCHLORIDE 300 mg/1 Details

    TRAMADOL HYDROCHLORIDE 300 mg/1

    TRAMADOL HYDROCHLORIDE is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is TRAMADOL HYDROCHLORIDE.

    Product Information

    NDC 70518-2795
    Product ID 70518-2795_04b6992d-c786-56c7-e063-6394a90ae8d0
    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 TRAMADOL HYDROCHLORIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name TRAMADOL HYDROCHLORIDE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 300
    Active Ingredient Units mg/1
    Substance Name TRAMADOL HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Full Opioid Agonists [MoA], Opioid Agonist [EPC]
    DEA Schedule CIV
    Marketing Category ANDA
    Application Number ANDA200503
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2795-00 (70518279500)

    NDC Package Code 70518-2795-0
    Billing NDC 70518279500
    Package 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2795-0)
    Marketing Start Date 2020-06-24
    NDC Exclude Flag N
    Pricing Information N/A