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    NDC 65162-0322-50 Niacin 750 mg/1 Details

    Niacin 750 mg/1

    Niacin is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. The primary component is NIACIN.

    Product Information

    NDC 65162-0322
    Product ID 65162-322_5f753958-58ea-4d23-bb9e-5455c519df92
    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 Niacin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Niacin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 750
    Active Ingredient Units mg/1
    Substance Name NIACIN
    Labeler Name Amneal Pharmaceuticals LLC
    Pharmaceutical Class Nicotinic Acid [EPC], Nicotinic Acids [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204178
    Listing Certified Through 2024-12-31

    Package

    NDC 65162-0322-50 (65162032250)

    NDC Package Code 65162-322-50
    Billing NDC 65162032250
    Package 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-322-50)
    Marketing Start Date 2015-12-11
    NDC Exclude Flag N
    Pricing Information N/A