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    NDC 71205-0931-60 Gabapentin 600 mg/1 Details

    Gabapentin 600 mg/1

    Gabapentin is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is GABAPENTIN.

    Product Information

    NDC 71205-0931
    Product ID 71205-931_26bd4975-008b-4029-b0da-3a75b0f7e0f4
    Associated GPIs 72600030000330
    GCN Sequence Number 041805
    GCN Sequence Number Description gabapentin TABLET 600 MG ORAL
    HIC3 H4B
    HIC3 Description ANTICONVULSANTS
    GCN 94624
    HICL Sequence Number 008831
    HICL Sequence Number Description GABAPENTIN
    Brand/Generic Generic
    Proprietary Name Gabapentin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Gabapentin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 600
    Active Ingredient Units mg/1
    Substance Name GABAPENTIN
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205101
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0931-60 (71205093160)

    NDC Package Code 71205-931-60
    Billing NDC 71205093160
    Package 60 TABLET in 1 BOTTLE (71205-931-60)
    Marketing Start Date 2021-04-22
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL b67b7865-df64-429a-9550-5333b9c713ea Details

    Revised: 4/2022