Search by Drug Name or NDC

    NDC 70518-2855-00 Duloxetine 30 mg/1 Details

    Duloxetine 30 mg/1

    Duloxetine is a ORAL CAPSULE, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is DULOXETINE HYDROCHLORIDE.

    Product Information

    NDC 70518-2855
    Product ID 70518-2855_04d84c8b-352c-daa7-e063-6294a90a35dc
    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 Duloxetine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Duloxetine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 30
    Active Ingredient Units mg/1
    Substance Name DULOXETINE HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203197
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2855-00 (70518285500)

    NDC Package Code 70518-2855-0
    Billing NDC 70518285500
    Package 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-2855-0)
    Marketing Start Date 2020-08-24
    NDC Exclude Flag N
    Pricing Information N/A