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    NDC 60760-0951-60 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 ST. MARY'S MEDICAL PARK PHARMACY. The primary component is DULOXETINE HYDROCHLORIDE.

    Product Information

    NDC 60760-0951
    Product ID 60760-951_0191629f-f9f4-6ad0-e063-6294a90a773f
    Associated GPIs
    GCN Sequence Number 057892
    GCN Sequence Number Description duloxetine HCl CAPSULE DR 30 MG ORAL
    HIC3 H7C
    HIC3 Description SEROTONIN-NOREPINEPHRINE REUPTAKE-INHIB (SNRIS)
    GCN 23162
    HICL Sequence Number 026521
    HICL Sequence Number Description DULOXETINE HCL
    Brand/Generic Generic
    Proprietary Name Duloxetine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Duloxetine Hydrochloride
    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 ST. MARY'S MEDICAL PARK PHARMACY
    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 ANDA090778
    Listing Certified Through 2024-12-31

    Package

    NDC 60760-0951-60 (60760095160)

    NDC Package Code 60760-951-60
    Billing NDC 60760095160
    Package 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-951-60)
    Marketing Start Date 2023-07-24
    NDC Exclude Flag N
    Pricing Information N/A