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    NDC 68382-0189-05 Dipyridamole 75 mg/1 Details

    Dipyridamole 75 mg/1

    Dipyridamole is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is DIPYRIDAMOLE.

    Product Information

    NDC 68382-0189
    Product ID 68382-189_8b638b19-214a-4a58-a336-656d690130e3
    Associated GPIs 85150030000330
    GCN Sequence Number 041700
    GCN Sequence Number Description dipyridamole TABLET 75 MG ORAL
    HIC3 M9P
    HIC3 Description PLATELET AGGREGATION INHIBITORS
    GCN 53143
    HICL Sequence Number 000168
    HICL Sequence Number Description DIPYRIDAMOLE
    Brand/Generic Generic
    Proprietary Name Dipyridamole
    Proprietary Name Suffix n/a
    Non-Proprietary Name Dipyridamole
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 75
    Active Ingredient Units mg/1
    Substance Name DIPYRIDAMOLE
    Labeler Name Zydus Pharmaceuticals USA Inc.
    Pharmaceutical Class Decreased Platelet Aggregation [PE], Platelet Aggregation Inhibitor [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA040874
    Listing Certified Through 2024-12-31

    Package

    NDC 68382-0189-05 (68382018905)

    NDC Package Code 68382-189-05
    Billing NDC 68382018905
    Package 500 TABLET, FILM COATED in 1 BOTTLE (68382-189-05)
    Marketing Start Date 2008-05-22
    NDC Exclude Flag N
    Pricing Information N/A