Search by Drug Name or NDC

    NDC 68788-7941-03 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 68788-7941
    Product ID 68788-7941_f5b04a0c-0266-45c5-8476-7e010d714b89
    Associated GPIs 72600030000140
    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 68788-7941-03 (68788794103)

    NDC Package Code 68788-7941-3
    Billing NDC 68788794103
    Package 30 CAPSULE in 1 BOTTLE (68788-7941-3)
    Marketing Start Date 2021-06-15
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 5706f117-01c0-4f24-95e3-871b0452053d Details

    Revised: 6/2022