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    NDC 55154-5633-00 Divalproex Sodium 500 mg/1 Details

    Divalproex Sodium 500 mg/1

    Divalproex Sodium is a ORAL TABLET, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Cardinal Health 107, LLC. The primary component is DIVALPROEX SODIUM.

    Product Information

    NDC 55154-5633
    Product ID 55154-5633_7255512a-f596-4e09-8f8c-7bed20447cde
    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 Divalproex Sodium
    Proprietary Name Suffix n/a
    Non-Proprietary Name Divalproex Sodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name DIVALPROEX SODIUM
    Labeler Name Cardinal Health 107, LLC
    Pharmaceutical Class Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078182
    Listing Certified Through 2024-12-31

    Package

    NDC 55154-5633-00 (55154563300)

    NDC Package Code 55154-5633-0
    Billing NDC 55154563300
    Package 10 BLISTER PACK in 1 BAG (55154-5633-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
    Marketing Start Date 2016-04-01
    NDC Exclude Flag N
    Pricing Information N/A