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    NDC 70934-0019-90 Sertraline Hydrochloride 100 mg/1 Details

    Sertraline Hydrochloride 100 mg/1

    Sertraline Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is SERTRALINE HYDROCHLORIDE.

    Product Information

    NDC 70934-0019
    Product ID 70934-019_d83d99fc-af98-c74b-e053-2a95a90aaf0a
    Associated GPIs 58160070100320
    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 Sertraline Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sertraline Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name SERTRALINE HYDROCHLORIDE
    Labeler Name Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    Pharmaceutical Class Cytochrome P450 2D6 Inhibitors [MoA], Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077206
    Listing Certified Through n/a

    Package

    NDC 70934-0019-90 (70934001990)

    NDC Package Code 70934-019-90
    Billing NDC 70934001990
    Package 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-019-90)
    Marketing Start Date 2020-07-13
    NDC Exclude Flag N
    Pricing Information N/A
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