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    NDC 59651-0020-05 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 Aurobindo Pharma Limited. The primary component is NIACIN.

    Product Information

    NDC 59651-0020
    Product ID 59651-020_8539231f-47da-402e-b05d-16c45cc3670c
    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 Aurobindo Pharma Limited
    Pharmaceutical Class Nicotinic Acid [EPC], Nicotinic Acids [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209236
    Listing Certified Through 2024-12-31

    Package

    NDC 59651-0020-05 (59651002005)

    NDC Package Code 59651-020-05
    Billing NDC 59651002005
    Package 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-020-05)
    Marketing Start Date 2018-02-01
    NDC Exclude Flag N
    Pricing Information N/A