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    NDC 65162-0323-50 Niacin 1000 mg/1 Details

    Niacin 1000 mg/1

    Niacin is a ORAL TABLET, 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 65162-0323
    Product ID 65162-323_b50aeac6-ecb7-4948-bd1b-fa3a3e19ebd8
    Associated GPIs 39450050000470
    GCN Sequence Number 033366
    GCN Sequence Number Description niacin TAB ER 24H 1000 MG ORAL
    HIC3 M4E
    HIC3 Description LIPOTROPICS
    GCN 42333
    HICL Sequence Number 001064
    HICL Sequence Number Description NIACIN
    Brand/Generic Generic
    Proprietary Name Niacin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Niacin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 1000
    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 ANDA203578
    Listing Certified Through 2024-12-31

    Package

    NDC 65162-0323-50 (65162032350)

    NDC Package Code 65162-323-50
    Billing NDC 65162032350
    Package 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-323-50)
    Marketing Start Date 2015-07-27
    NDC Exclude Flag N
    Pricing Information N/A