Search by Drug Name or NDC

    NDC 68788-7135-01 GABAPENTIN 400 mg/1 Details

    GABAPENTIN 400 mg/1

    GABAPENTIN is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is GABAPENTIN.

    Product Information

    NDC 68788-7135
    Product ID 68788-7135_b5d71771-f1aa-435f-bfaa-68b3288d51cf
    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 GABAPENTIN
    Proprietary Name Suffix n/a
    Non-Proprietary Name GABAPENTIN
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 400
    Active Ingredient Units mg/1
    Substance Name GABAPENTIN
    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 ANDA090007
    Listing Certified Through 2023-12-31

    Package

    NDC 68788-7135-01 (68788713501)

    NDC Package Code 68788-7135-1
    Billing NDC 68788713501
    Package 100 CAPSULE in 1 BOTTLE (68788-7135-1)
    Marketing Start Date 2020-06-02
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL e9596cc1-eff1-4df1-a011-994fd22acf22 Details

    Revised: 6/2022