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    NDC 43063-0671-30 Etodolac 500 mg/1 Details

    Etodolac 500 mg/1

    Etodolac is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is ETODOLAC.

    Product Information

    NDC 43063-0671
    Product ID 43063-671_f98acaf6-d181-3c0c-e053-6394a90a62fe
    Associated GPIs 66100008000320
    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 Etodolac
    Proprietary Name Suffix n/a
    Non-Proprietary Name Etodolac
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name ETODOLAC
    Labeler Name PD-Rx Pharmaceuticals, Inc.
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076004
    Listing Certified Through 2024-12-31

    Package

    NDC 43063-0671-30 (43063067130)

    NDC Package Code 43063-671-30
    Billing NDC 43063067130
    Package 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-671-30)
    Marketing Start Date 2018-01-16
    NDC Exclude Flag N
    Pricing Information N/A