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    NDC 51655-0176-84 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 NORTHWIND PHARMACEUTICALS. The primary component is DICLOFENAC SODIUM.

    Product Information

    NDC 51655-0176
    Product ID 51655-176_f2b4948d-d325-4b84-e053-2a95a90a7d12
    Associated GPIs
    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 Delayed Release
    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 NORTHWIND PHARMACEUTICALS
    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 ANDA075185
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0176-84 (51655017684)

    NDC Package Code 51655-176-84
    Billing NDC 51655017684
    Package 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-176-84)
    Marketing Start Date 2020-09-29
    NDC Exclude Flag N
    Pricing Information N/A