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    NDC 70518-2527-00 divalproex sodium 125 mg/1 Details

    divalproex sodium 125 mg/1

    divalproex sodium is a ORAL CAPSULE, COATED PELLETS in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is DIVALPROEX SODIUM.

    Product Information

    NDC 70518-2527
    Product ID 70518-2527_044b3ef1-04cf-52e1-e063-6294a90a12d2
    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 CAPSULE, COATED PELLETS
    Route ORAL
    Active Ingredient Strength 125
    Active Ingredient Units mg/1
    Substance Name DIVALPROEX SODIUM
    Labeler Name REMEDYREPACK INC.
    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 ANDA078919
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2527-00 (70518252700)

    NDC Package Code 70518-2527-0
    Billing NDC 70518252700
    Package 100 POUCH in 1 BOX (70518-2527-0) / 1 CAPSULE, COATED PELLETS in 1 POUCH (70518-2527-1)
    Marketing Start Date 2020-01-06
    NDC Exclude Flag N
    Pricing Information N/A