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    NDC 68180-0460-06 Minocycline Hydrochloride 55 mg/1 Details

    Minocycline Hydrochloride 55 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 68180-0460
    Product ID 68180-460_ad320f99-9382-4ef0-b6b6-86542020555a
    Associated GPIs 04000040107522
    GCN Sequence Number 066683
    GCN Sequence Number Description minocycline HCl TAB ER 24H 55 MG ORAL
    HIC3 W1C
    HIC3 Description TETRACYCLINE ANTIBIOTICS
    GCN 29040
    HICL Sequence Number 004015
    HICL Sequence Number Description MINOCYCLINE HCL
    Brand/Generic Generic
    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 55
    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 68180-0460-06 (68180046006)

    NDC Package Code 68180-460-06
    Billing NDC 68180046006
    Package 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-460-06)
    Marketing Start Date 2019-02-22
    NDC Exclude Flag N
    Pricing Information N/A