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    NDC 70934-0461-20 tramadol hydrochloride 50 mg/1 Details

    tramadol hydrochloride 50 mg/1

    tramadol hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. dba Northwind Pharmaceuticals. The primary component is TRAMADOL HYDROCHLORIDE.

    Product Information

    NDC 70934-0461
    Product ID 70934-461_c2b1a7cb-ca62-dc2b-e053-2995a90a32ed
    Associated GPIs
    GCN Sequence Number 023139
    GCN Sequence Number Description tramadol HCl TABLET 50 MG ORAL
    HIC3 H3A
    HIC3 Description OPIOID ANALGESICS
    GCN 07221
    HICL Sequence Number 008317
    HICL Sequence Number Description TRAMADOL HCL
    Brand/Generic Generic
    Proprietary Name tramadol hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name tramadol hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name TRAMADOL HYDROCHLORIDE
    Labeler Name Denton Pharma, Inc. dba Northwind Pharmaceuticals
    Pharmaceutical Class Full Opioid Agonists [MoA], Opioid Agonist [EPC]
    DEA Schedule CIV
    Marketing Category ANDA
    Application Number ANDA075964
    Listing Certified Through n/a

    Package

    NDC 70934-0461-20 (70934046120)

    NDC Package Code 70934-461-20
    Billing NDC 70934046120
    Package 20 TABLET in 1 BOTTLE, PLASTIC (70934-461-20)
    Marketing Start Date 2019-10-31
    NDC Exclude Flag N
    Pricing Information N/A