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    NDC 71205-0514-90 Gabapentin 800 mg/1 Details

    Gabapentin 800 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 71205-0514
    Product ID 71205-514_dca73902-4c06-4304-a5a4-b289b020cee4
    Associated GPIs 72600030000340
    GCN Sequence Number 041806
    GCN Sequence Number Description gabapentin TABLET 800 MG ORAL
    HIC3 H4B
    HIC3 Description ANTICONVULSANTS
    GCN 94447
    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 800
    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 71205-0514-90 (71205051490)

    NDC Package Code 71205-514-90
    Billing NDC 71205051490
    Package 90 TABLET in 1 BOTTLE (71205-514-90)
    Marketing Start Date 2020-12-09
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 2b76955c-52a4-4026-b286-3da1112fe989 Details

    Revised: 4/2022