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    NDC 70710-1543-08 ZALDYON 800 mg/1 Details

    ZALDYON 800 mg/1

    ZALDYON is a ORAL TABLET, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is MESALAMINE.

    Product Information

    NDC 70710-1543
    Product ID 70710-1543_dcbddcc0-3d6a-4c4e-817c-699e31171810
    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 ZALDYON
    Proprietary Name Suffix n/a
    Non-Proprietary Name mesalamine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 800
    Active Ingredient Units mg/1
    Substance Name MESALAMINE
    Labeler Name Zydus Pharmaceuticals USA Inc.
    Pharmaceutical Class Aminosalicylate [EPC], Aminosalicylic Acids [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203286
    Listing Certified Through 2024-12-31

    Package

    NDC 70710-1543-08 (70710154308)

    NDC Package Code 70710-1543-8
    Billing NDC 70710154308
    Package 180 TABLET, DELAYED RELEASE in 1 BOTTLE (70710-1543-8)
    Marketing Start Date 2019-01-17
    NDC Exclude Flag N
    Pricing Information N/A