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    NDC 51655-0253-52 celecoxib 200 mg/1 Details

    celecoxib 200 mg/1

    celecoxib is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. The primary component is CELECOXIB.

    Product Information

    NDC 51655-0253
    Product ID 51655-253_088f73fd-a224-ea44-e063-6294a90acb49
    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 celecoxib
    Proprietary Name Suffix n/a
    Non-Proprietary Name celecoxib
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name CELECOXIB
    Labeler Name Northwind Pharmaceuticals, LLC
    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 ANDA204590
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0253-52 (51655025352)

    NDC Package Code 51655-253-52
    Billing NDC 51655025352
    Package 30 CAPSULE in 1 BOTTLE, PLASTIC (51655-253-52)
    Marketing Start Date 2020-11-04
    NDC Exclude Flag N
    Pricing Information N/A