Search by Drug Name or NDC

    NDC 68180-0760-01 Amlodipine Besylate and Benazepril Hydrochloride 10; 40 mg/1; mg/1 Details

    Amlodipine Besylate and Benazepril Hydrochloride 10; 40 mg/1; mg/1

    Amlodipine Besylate and Benazepril Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. The primary component is AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE.

    Product Information

    NDC 68180-0760
    Product ID 68180-760_3f88556b-447a-40c5-917a-e50e0d818c5a
    Associated GPIs 36991502200160
    GCN Sequence Number 060723
    GCN Sequence Number Description amlodipine besylate/benazepril CAPSULE 10 MG-40MG ORAL
    HIC3 A4K
    HIC3 Description ACE INHIBITOR-CALCIUM CHANNEL BLOCKER COMBINATION
    GCN 26950
    HICL Sequence Number 010041
    HICL Sequence Number Description AMLODIPINE BESYLATE/BENAZEPRIL HCL
    Brand/Generic Generic
    Proprietary Name Amlodipine Besylate and Benazepril Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Amlodipine Besylate and Benazepril Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 10; 40
    Active Ingredient Units mg/1; mg/1
    Substance Name AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
    Labeler Name Lupin Pharmaceuticals, Inc.
    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], Decreased Blood Pressure [PE], Dihydropyridine Calcium Ch
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078466
    Listing Certified Through 2024-12-31

    Package

    NDC 68180-0760-01 (68180076001)

    NDC Package Code 68180-760-01
    Billing NDC 68180076001
    Package 100 CAPSULE in 1 BOTTLE (68180-760-01)
    Marketing Start Date 2011-07-05
    NDC Exclude Flag N
    Pricing Information N/A