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    NDC 68180-0379-01 Minocycline Hydrochloride 45 mg/1 Details

    Minocycline Hydrochloride 45 mg/1

    Minocycline Hydrochloride 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 MINOCYCLINE HYDROCHLORIDE.

    Product Information

    NDC 68180-0379
    Product ID 68180-379_ad320f99-9382-4ef0-b6b6-86542020555a
    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 Minocycline Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Minocycline Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 45
    Active Ingredient Units mg/1
    Substance Name MINOCYCLINE HYDROCHLORIDE
    Labeler Name Lupin Pharmaceuticals, Inc.
    Pharmaceutical Class Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA091424
    Listing Certified Through 2024-12-31

    Package

    NDC 68180-0379-01 (68180037901)

    NDC Package Code 68180-379-01
    Billing NDC 68180037901
    Package 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-379-01)
    Marketing Start Date 2012-02-14
    NDC Exclude Flag N
    Pricing Information N/A