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    NDC 68382-0551-05 minocycline hydrochloride 80 mg/1 Details

    minocycline hydrochloride 80 mg/1

    minocycline hydrochloride is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals (USA) Inc.. The primary component is MINOCYCLINE HYDROCHLORIDE.

    Product Information

    NDC 68382-0551
    Product ID 68382-551_fe782f9a-84d1-4e4a-ad19-83b869ee07ad
    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 80
    Active Ingredient Units mg/1
    Substance Name MINOCYCLINE HYDROCHLORIDE
    Labeler Name Zydus Pharmaceuticals (USA) Inc.
    Pharmaceutical Class Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203553
    Listing Certified Through 2024-12-31

    Package

    NDC 68382-0551-05 (68382055105)

    NDC Package Code 68382-551-05
    Billing NDC 68382055105
    Package 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-551-05)
    Marketing Start Date 2018-03-07
    NDC Exclude Flag N
    Pricing Information N/A