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    NDC 71205-0025-90 CARBAMAZEPINE 200 mg/1 Details

    CARBAMAZEPINE 200 mg/1

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

    Product Information

    NDC 71205-0025
    Product ID 71205-025_9a099066-50bb-4651-bce7-5e1dc8e2e5b1
    Associated GPIs 72600020000305
    GCN Sequence Number 004558
    GCN Sequence Number Description carbamazepine TABLET 200 MG ORAL
    HIC3 H4B
    HIC3 Description ANTICONVULSANTS
    GCN 17450
    HICL Sequence Number 001893
    HICL Sequence Number Description CARBAMAZEPINE
    Brand/Generic Generic
    Proprietary Name CARBAMAZEPINE
    Proprietary Name Suffix n/a
    Non-Proprietary Name CARBAMAZEPINE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name CARBAMAZEPINE
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 3A4 Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mo
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA075948
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0025-90 (71205002590)

    NDC Package Code 71205-025-90
    Billing NDC 71205002590
    Package 90 TABLET in 1 BOTTLE (71205-025-90)
    Marketing Start Date 2018-05-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL bf61798e-c07e-4959-909a-2b4c2c83b532 Details

    Revised: 10/2019