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    NDC 27854-0170-01 AnaDent 220 mg/1 Details

    AnaDent 220 mg/1

    AnaDent is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Belmora LLC. The primary component is NAPROXEN SODIUM.

    Product Information

    NDC 27854-0170
    Product ID 27854-170_e8ea9ae2-375a-4bb9-b807-4c101ce9f3d7
    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 AnaDent
    Proprietary Name Suffix n/a
    Non-Proprietary Name Naproxen Sodium
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 220
    Active Ingredient Units mg/1
    Substance Name NAPROXEN SODIUM
    Labeler Name Belmora 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 ANDA204872
    Listing Certified Through 2024-12-31

    Package

    NDC 27854-0170-01 (27854017001)

    NDC Package Code 27854-170-01
    Billing NDC 27854017001
    Package 1 BOTTLE, PLASTIC in 1 CARTON (27854-170-01) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    Marketing Start Date 2017-01-23
    NDC Exclude Flag N
    Pricing Information N/A