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    NDC 65862-0561-30 Olanzapine 2.5 mg/1 Details

    Olanzapine 2.5 mg/1

    Olanzapine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is OLANZAPINE.

    Product Information

    NDC 65862-0561
    Product ID 65862-561_ed955156-766b-4bdb-a4f8-a56550c7f263
    Associated GPIs 59157060000305
    GCN Sequence Number 029077
    GCN Sequence Number Description olanzapine TABLET 2.5 MG ORAL
    HIC3 H7T
    HIC3 Description ANTIPSYCHOTIC,ATYPICAL,DOPAMINE,SEROTONIN ANTAGNST
    GCN 15084
    HICL Sequence Number 011814
    HICL Sequence Number Description OLANZAPINE
    Brand/Generic Generic
    Proprietary Name Olanzapine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Olanzapine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 2.5
    Active Ingredient Units mg/1
    Substance Name OLANZAPINE
    Labeler Name Aurobindo Pharma Limited
    Pharmaceutical Class Atypical Antipsychotic [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202050
    Listing Certified Through 2024-12-31

    Package

    NDC 65862-0561-30 (65862056130)

    NDC Package Code 65862-561-30
    Billing NDC 65862056130
    Package 30 TABLET in 1 BOTTLE (65862-561-30)
    Marketing Start Date 2012-04-23
    NDC Exclude Flag N
    Pricing Information
    Price Per Unit 0.08685
    Pricing Unit EA
    Effective Date 2022-11-23
    NDC Description OLANZAPINE 2.5 MG TABLET
    Pharmacy Type Indicator C/I
    OTC N
    Explanation Code 1
    Classification for Rate Setting G
    As of Date 2022-11-23
    This pricing file, entitled the NADAC (National Average Drug Acquisition Cost) files, provide state Medicaid agencies with covered outpatient drug prices by averaging survey invoice prices from retail community pharmacies across the United States. These pharmacies include independent retail community pharmacies and chain pharmacies. The prices are updated on a weekly and monthly basis

    Standard Product Labeling (SPL)/Prescribing Information SPL 636665be-9d7e-443a-8134-e8cc47e6ba24 Details

    Revised: 11/2022