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    NDC 68788-6388-01 Diclofenac Sodium 100 mg/1 Details

    Diclofenac Sodium 100 mg/1

    Diclofenac Sodium is a ORAL TABLET, FILM COATED, EXTENDED 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 68788-6388
    Product ID 68788-6388_cd166268-60a8-4612-b407-d6aa4084e21b
    Associated GPIs 66100007207530
    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, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 100
    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 ANDA075492
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-6388-01 (68788638801)

    NDC Package Code 68788-6388-1
    Billing NDC 68788638801
    Package 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-6388-1)
    Marketing Start Date 2016-05-05
    NDC Exclude Flag N
    Pricing Information N/A