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    NDC 00069-2190-30 Caduet 5; 40 mg/1; mg/1 Details

    Caduet 5; 40 mg/1; mg/1

    Caduet is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Pfizer Laboratories Div Pfizer Inc. The primary component is AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE.

    Product Information

    NDC 00069-2190
    Product ID 0069-2190_9c800a70-9fd4-427c-b848-c65fff86f7e6
    Associated GPIs 40992502150330
    GCN Sequence Number 053691
    GCN Sequence Number Description amlodipine/atorvastatin TABLET 5 MG-40 MG ORAL
    HIC3 M4I
    HIC3 Description ANTIHYPERLIPID- HMG-COA RI-CALCIUM CHANNEL BLOCKER
    GCN 21393
    HICL Sequence Number 025951
    HICL Sequence Number Description AMLODIPINE BESYLATE/ATORVASTATIN CALCIUM
    Brand/Generic Brand
    Proprietary Name Caduet
    Proprietary Name Suffix n/a
    Non-Proprietary Name amlodipine besylate and atorvastatin calcium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 5; 40
    Active Ingredient Units mg/1; mg/1
    Substance Name AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE
    Labeler Name Pfizer Laboratories Div Pfizer Inc
    Pharmaceutical Class Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021540
    Listing Certified Through 2024-12-31

    Package

    NDC 00069-2190-30 (00069219030)

    NDC Package Code 0069-2190-30
    Billing NDC 00069219030
    Package 30 TABLET, FILM COATED in 1 BOTTLE (0069-2190-30)
    Marketing Start Date 2004-01-30
    NDC Exclude Flag N
    Pricing Information N/A