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    NDC 63629-9214-01 Minocycline Hydrochloride 80 mg/1 Details

    Minocycline Hydrochloride 80 mg/1

    Minocycline Hydrochloride is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is MINOCYCLINE HYDROCHLORIDE.

    Product Information

    NDC 63629-9214
    Product ID 63629-9214_42357d96-74ef-4de3-a647-bdcb52aaa29e
    Associated GPIs 04000040107528
    GCN Sequence Number 066684
    GCN Sequence Number Description minocycline HCl TAB ER 24H 80 MG ORAL
    HIC3 W1C
    HIC3 Description TETRACYCLINE ANTIBIOTICS
    GCN 29044
    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, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 80
    Active Ingredient Units mg/1
    Substance Name MINOCYCLINE HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204453
    Listing Certified Through 2024-12-31

    Package

    NDC 63629-9214-01 (63629921401)

    NDC Package Code 63629-9214-1
    Billing NDC 63629921401
    Package 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9214-1)
    Marketing Start Date 2022-03-02
    NDC Exclude Flag N
    Pricing Information N/A