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    NDC 99207-0467-30 Solodyn 105 mg/1 Details

    Solodyn 105 mg/1

    Solodyn is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bausch Health US LLC. The primary component is MINOCYCLINE HYDROCHLORIDE.

    Product Information

    NDC 99207-0467
    Product ID 99207-467_56aa28d4-9493-4cfb-ac2e-794105f6be64
    Associated GPIs 04000040107533
    GCN Sequence Number 066685
    GCN Sequence Number Description minocycline HCl TAB ER 24H 105 MG ORAL
    HIC3 W1C
    HIC3 Description TETRACYCLINE ANTIBIOTICS
    GCN 29045
    HICL Sequence Number 004015
    HICL Sequence Number Description MINOCYCLINE HCL
    Brand/Generic Brand
    Proprietary Name Solodyn
    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 105
    Active Ingredient Units mg/1
    Substance Name MINOCYCLINE HYDROCHLORIDE
    Labeler Name Bausch Health US LLC
    Pharmaceutical Class Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA050808
    Listing Certified Through 2024-12-31

    Package

    NDC 99207-0467-30 (99207046730)

    NDC Package Code 99207-467-30
    Billing NDC 99207046730
    Package 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (99207-467-30)
    Marketing Start Date 2010-09-27
    NDC Exclude Flag N
    Pricing Information N/A