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    NDC 50090-2338-00 Quetiapine 100 mg/1 Details

    Quetiapine 100 mg/1

    Quetiapine is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is QUETIAPINE FUMARATE.

    Product Information

    NDC 50090-2338
    Product ID 50090-2338_e8b4d5ba-e056-4842-8a2c-c50116f7f0e2
    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 Quetiapine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Quetiapine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name QUETIAPINE FUMARATE
    Labeler Name A-S Medication Solutions
    Pharmaceutical Class Atypical Antipsychotic [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202152
    Listing Certified Through 2024-12-31

    Package

    NDC 50090-2338-00 (50090233800)

    NDC Package Code 50090-2338-0
    Billing NDC 50090233800
    Package 30 TABLET, FILM COATED in 1 BOTTLE (50090-2338-0)
    Marketing Start Date 2016-03-29
    NDC Exclude Flag N
    Pricing Information N/A