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    NDC 68788-7866-06 OXCARBAZEPINE 600 mg/1 Details

    OXCARBAZEPINE 600 mg/1

    OXCARBAZEPINE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is OXCARBAZEPINE.

    Product Information

    NDC 68788-7866
    Product ID 68788-7866_2cafffd2-984b-490c-b9ee-c6dc0eefd01c
    Associated GPIs 72600046000340
    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 OXCARBAZEPINE
    Proprietary Name Suffix n/a
    Non-Proprietary Name OXCARBAZEPINE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 600
    Active Ingredient Units mg/1
    Substance Name OXCARBAZEPINE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078069
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7866-06 (68788786606)

    NDC Package Code 68788-7866-6
    Billing NDC 68788786606
    Package 60 TABLET, FILM COATED in 1 BOTTLE (68788-7866-6)
    Marketing Start Date 2021-02-15
    NDC Exclude Flag N
    Pricing Information N/A