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    NDC 68788-8193-03 Diclofenac Sodium 75 mg/1 Details

    Diclofenac Sodium 75 mg/1

    Diclofenac Sodium is a ORAL TABLET, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is DICLOFENAC SODIUM.

    Product Information

    NDC 68788-8193
    Product ID 68788-8193_c336c770-0aec-4a50-8e06-7ca4c178e9d4
    Associated GPIs 66100007200630
    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 Diclofenac Sodium
    Proprietary Name Suffix n/a
    Non-Proprietary Name Diclofenac Sodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 75
    Active Ingredient Units mg/1
    Substance Name DICLOFENAC SODIUM
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077863
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-8193-03 (68788819303)

    NDC Package Code 68788-8193-3
    Billing NDC 68788819303
    Package 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8193-3)
    Marketing Start Date 2022-05-16
    NDC Exclude Flag N
    Pricing Information N/A