Search by Drug Name or NDC

    NDC 69790-0620-33 ULINE Aspirin 325 mg/1 Details

    ULINE Aspirin 325 mg/1

    ULINE Aspirin is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by ULINE. The primary component is ASPIRIN.

    Product Information

    NDC 69790-0620
    Product ID 69790-620_da2ea7d4-4a9e-565c-e053-2995a90a2127
    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 ULINE Aspirin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Aspirin
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 325
    Active Ingredient Units mg/1
    Substance Name ASPIRIN
    Labeler Name ULINE
    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 NOT FINAL
    Application Number part343
    Listing Certified Through 2023-12-31

    Package

    NDC 69790-0620-33 (69790062033)

    NDC Package Code 69790-620-33
    Billing NDC 69790062033
    Package 50 PACKET in 1 BOX (69790-620-33) / 2 TABLET, COATED in 1 PACKET
    Marketing Start Date 2021-02-05
    NDC Exclude Flag N
    Pricing Information N/A