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    NDC 70518-2960-02 Gabapentin 600 mg/1 Details

    Gabapentin 600 mg/1

    Gabapentin is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is GABAPENTIN.

    Product Information

    NDC 70518-2960
    Product ID 70518-2960_03bf4af4-10a1-4980-e063-6294a90abcd4
    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 TABLET, COATED
    Route ORAL
    Active Ingredient Strength 600
    Active Ingredient Units mg/1
    Substance Name GABAPENTIN
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Decreased Central Nervous System Disorganized Electrical Activity [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207057
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2960-02 (70518296002)

    NDC Package Code 70518-2960-2
    Billing NDC 70518296002
    Package 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2960-2)
    Marketing Start Date 2022-07-29
    NDC Exclude Flag N
    Pricing Information N/A