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    NDC 50804-0157-12 Aspirin 325 mg/1 Details

    Aspirin 325 mg/1

    Aspirin is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Geiss, Destin & Dunn Inc.. The primary component is ASPIRIN.

    Product Information

    NDC 50804-0157
    Product ID 50804-157_f09ea7f2-4b3c-4abd-b66d-bc1b048b8013
    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 Aspirin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Aspirin
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 325
    Active Ingredient Units mg/1
    Substance Name ASPIRIN
    Labeler Name Geiss, Destin & Dunn Inc.
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M013
    Listing Certified Through 2024-12-31

    Package

    NDC 50804-0157-12 (50804015712)

    NDC Package Code 50804-157-12
    Billing NDC 50804015712
    Package 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50804-157-12)
    Marketing Start Date 2023-05-12
    NDC Exclude Flag N
    Pricing Information N/A