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    NDC 68180-0222-02 NIACIN 750 mg/1 Details

    NIACIN 750 mg/1

    NIACIN is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. The primary component is NIACIN.

    Product Information

    NDC 68180-0222
    Product ID 68180-222_309a40e8-333f-478a-8a94-beff7f3ca5b2
    Associated GPIs 39450050000460
    GCN Sequence Number 033365
    GCN Sequence Number Description niacin TAB ER 24H 750 MG ORAL
    HIC3 M4E
    HIC3 Description LIPOTROPICS
    GCN 42332
    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 750
    Active Ingredient Units mg/1
    Substance Name NIACIN
    Labeler Name Lupin Pharmaceuticals, Inc.
    Pharmaceutical Class Nicotinic Acid [EPC], Nicotinic Acids [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090892
    Listing Certified Through 2024-12-31

    Package

    NDC 68180-0222-02 (68180022202)

    NDC Package Code 68180-222-02
    Billing NDC 68180022202
    Package 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-222-02)
    Marketing Start Date 2014-03-20
    NDC Exclude Flag N
    Pricing Information N/A