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    NDC 68462-0294-01 Trandolapril and Verapamil Hydrochloride 1; 240 mg/1; mg/1 Details

    Trandolapril and Verapamil Hydrochloride 1; 240 mg/1; mg/1

    Trandolapril and Verapamil Hydrochloride is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Glenmark Pharmaceuticals Inc., USA. The primary component is TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE.

    Product Information

    NDC 68462-0294
    Product ID 68462-294_a3d55a5c-1f69-456d-a01a-60c18b186264
    Associated GPIs 36991502700420
    GCN Sequence Number 029252
    GCN Sequence Number Description trandolapril/verapamil HCl TAB BP 24H 1MG-240 MG ORAL
    HIC3 A4K
    HIC3 Description ACE INHIBITOR-CALCIUM CHANNEL BLOCKER COMBINATION
    GCN 32112
    HICL Sequence Number 012230
    HICL Sequence Number Description TRANDOLAPRIL/VERAPAMIL HCL
    Brand/Generic Generic
    Proprietary Name Trandolapril and Verapamil Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Trandolapril and Verapamil Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 1; 240
    Active Ingredient Units mg/1; mg/1
    Substance Name TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE
    Labeler Name Glenmark Pharmaceuticals Inc., USA
    Pharmaceutical Class Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], P-Glycoprotein Inhi
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA079135
    Listing Certified Through 2025-12-31

    Package

    NDC 68462-0294-01 (68462029401)

    NDC Package Code 68462-294-01
    Billing NDC 68462029401
    Package 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-294-01)
    Marketing Start Date 2015-02-25
    NDC Exclude Flag N
    Pricing Information N/A