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    NDC 70934-0630-90 Escitalopram 10 mg/1 Details

    Escitalopram 10 mg/1

    Escitalopram 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 ESCITALOPRAM OXALATE.

    Product Information

    NDC 70934-0630
    Product ID 70934-630_d4af8193-5249-64d3-e053-2a95a90ab049
    Associated GPIs 58160034100320
    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 Escitalopram
    Proprietary Name Suffix n/a
    Non-Proprietary Name Escitalopram
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name ESCITALOPRAM OXALATE
    Labeler Name Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078032
    Listing Certified Through n/a

    Package

    NDC 70934-0630-90 (70934063090)

    NDC Package Code 70934-630-90
    Billing NDC 70934063090
    Package 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-630-90)
    Marketing Start Date 2020-03-18
    NDC Exclude Flag N
    Pricing Information N/A
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