NDC 30698-453

Lotensin HCT

Benazepril Hydrochloride And Hydrochlorothiazide

Lotensin HCT is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Validus Pharmaceuticals Llc. The primary component is Benazepril Hydrochloride; Hydrochlorothiazide.

Product ID30698-453_40bb04ea-bdb6-43d2-b734-6517157b9319
NDC30698-453
Product TypeHuman Prescription Drug
Proprietary NameLotensin HCT
Generic NameBenazepril Hydrochloride And Hydrochlorothiazide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1992-05-30
Marketing CategoryNDA / NDA
Application NumberNDA020033
Labeler NameValidus Pharmaceuticals LLC
Substance NameBENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Active Ingredient Strength20 mg/1; mg/1
Pharm ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 30698-453-01

100 TABLET in 1 BOTTLE (30698-453-01)
Marketing Start Date1992-05-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 30698-453-01 [30698045301]

Lotensin HCT TABLET
Marketing CategoryNDA
Application NumberNDA020033
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1992-05-30

Drug Details

Active Ingredients

IngredientStrength
BENAZEPRIL HYDROCHLORIDE20 mg/1

OpenFDA Data

SPL SET ID:94c4536f-e28e-48b1-8336-b3939917e99d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 898366
  • 898367
  • 898376
  • 898362
  • 898372
  • 898371
    • UPC Code
  • 0330698454015
  • 0330698453018
  • 0330698452011

    • Pharmacological Class

    • Angiotensin Converting Enzyme Inhibitor [EPC]
    • Angiotensin-converting Enzyme Inhibitors [MoA]
    • Decreased Blood Pressure [PE]
    • Increased Diuresis [PE]
    • Thiazide Diuretic [EPC]
    • Thiazides [CS]

    NDC Crossover Matching brand name "Lotensin HCT" or generic name "Benazepril Hydrochloride And Hydrochlorothiazide"

    NDCBrand NameGeneric Name
    30698-452Lotensin HCTbenazepril hydrochloride and hydrochlorothiazide
    30698-453Lotensin HCTbenazepril hydrochloride and hydrochlorothiazide
    30698-454Lotensin HCTLotensin HCT
    0185-0211Benazepril Hydrochloride and HydrochlorothiazideBenazepril Hydrochloride and Hydrochlorothiazide
    0185-0236Benazepril Hydrochloride and HydrochlorothiazideBenazepril Hydrochloride and Hydrochlorothiazide
    0185-0277Benazepril Hydrochloride and HydrochlorothiazideBenazepril Hydrochloride and Hydrochlorothiazide
    0185-0325Benazepril Hydrochloride and HydrochlorothiazideBenazepril Hydrochloride and Hydrochlorothiazide
    0378-4725Benazepril Hydrochloride and Hydrochlorothiazidebenazepril hydrochloride and hydrochlorothiazide
    0378-4735Benazepril Hydrochloride and Hydrochlorothiazidebenazepril hydrochloride and hydrochlorothiazide
    0378-4745Benazepril Hydrochloride and Hydrochlorothiazidebenazepril hydrochloride and hydrochlorothiazide
    0378-4775Benazepril Hydrochloride and Hydrochlorothiazidebenazepril hydrochloride and hydrochlorothiazide
    0574-0227benazepril hydrochloride and hydrochlorothiazidebenazepril hydrochloride and hydrochlorothiazide
    0574-0228benazepril hydrochloride and hydrochlorothiazidebenazepril hydrochloride and hydrochlorothiazide
    0574-0229benazepril hydrochloride and hydrochlorothiazidebenazepril hydrochloride and hydrochlorothiazide
    0832-0483Benazepril Hydrochloride and HydrochlorothiazideBenazepril Hydrochloride and Hydrochlorothiazide
    0832-0484Benazepril Hydrochloride and HydrochlorothiazideBenazepril Hydrochloride and Hydrochlorothiazide
    0832-0485Benazepril Hydrochloride and HydrochlorothiazideBenazepril Hydrochloride and Hydrochlorothiazide

    Trademark Results [Lotensin HCT]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    LOTENSIN HCT
    LOTENSIN HCT
    74134117 1882770 Live/Registered
    NOVARTIS PHARMACEUTICALS CORPORATION
    1991-01-28
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