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    NDC 71335-0090-01 OXCARBAZEPINE 300 mg/1 Details

    OXCARBAZEPINE 300 mg/1

    OXCARBAZEPINE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is OXCARBAZEPINE.

    Product Information

    NDC 71335-0090
    Product ID 71335-0090_c1c29e18-455d-4321-b993-cbfb812e638c
    Associated GPIs
    GCN Sequence Number 027779
    GCN Sequence Number Description oxcarbazepine TABLET 300 MG ORAL
    HIC3 H4B
    HIC3 Description ANTICONVULSANTS
    GCN 21721
    HICL Sequence Number 011735
    HICL Sequence Number Description OXCARBAZEPINE
    Brand/Generic Generic
    Proprietary Name OXCARBAZEPINE
    Proprietary Name Suffix n/a
    Non-Proprietary Name OXCARBAZEPINE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 300
    Active Ingredient Units mg/1
    Substance Name OXCARBAZEPINE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078069
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0090-01 (71335009001)

    NDC Package Code 71335-0090-1
    Billing NDC 71335009001
    Package 30 TABLET, FILM COATED in 1 BOTTLE (71335-0090-1)
    Marketing Start Date 2020-06-04
    NDC Exclude Flag N
    Pricing Information N/A