NDC 68788-7248

Benazepril Hydrochloride

Benazepril Hydrochloride

Benazepril Hydrochloride is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is Benazepril Hydrochloride.

Product ID68788-7248_2e3e4d82-04d8-4ca1-b5c3-95e0aab14041
NDC68788-7248
Product TypeHuman Prescription Drug
Proprietary NameBenazepril Hydrochloride
Generic NameBenazepril Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2018-08-27
Marketing CategoryANDA / ANDA
Application NumberANDA078212
Labeler NamePreferred Pharmaceuticals Inc.
Substance NameBENAZEPRIL HYDROCHLORIDE
Active Ingredient Strength40 mg/1
Pharm ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68788-7248-8

120 TABLET, FILM COATED in 1 BOTTLE (68788-7248-8)
Marketing Start Date2018-08-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-7248-3 [68788724803]

Benazepril Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078212
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-08-27
Marketing End Date2020-03-31

NDC 68788-7248-8 [68788724808]

Benazepril Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078212
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-08-27
Marketing End Date2020-03-31

NDC 68788-7248-6 [68788724806]

Benazepril Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078212
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-08-27
Marketing End Date2020-03-31

NDC 68788-7248-9 [68788724809]

Benazepril Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078212
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-08-27
Marketing End Date2020-03-31

NDC 68788-7248-1 [68788724801]

Benazepril Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078212
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-08-27
Marketing End Date2020-03-31

Drug Details

Active Ingredients

IngredientStrength
BENAZEPRIL HYDROCHLORIDE40 mg/1

OpenFDA Data

SPL SET ID:2e3e4d82-04d8-4ca1-b5c3-95e0aab14041
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 898719

    • Pharmacological Class

    • Angiotensin Converting Enzyme Inhibitor [EPC]
    • Angiotensin-converting Enzyme Inhibitors [MoA]
    • Decreased Blood Pressure [PE]

    NDC Crossover Matching brand name "Benazepril Hydrochloride" or generic name "Benazepril Hydrochloride"

    NDCBrand NameGeneric Name
    0185-0053Benazepril HydrochlorideBenazepril Hydrochloride
    0185-0505Benazepril HydrochlorideBenazepril Hydrochloride
    0185-0820Benazepril HydrochlorideBenazepril Hydrochloride
    0378-0441Benazepril Hydrochloridebenazepril hydrochloride
    0378-0443Benazepril Hydrochloridebenazepril hydrochloride
    0378-0444Benazepril Hydrochloridebenazepril hydrochloride
    0378-0447Benazepril Hydrochloridebenazepril hydrochloride
    10544-554Benazepril HydrochlorideBenazepril Hydrochloride
    10544-561Benazepril HydrochlorideBenazepril Hydrochloride
    10544-566Benazepril HydrochlorideBenazepril Hydrochloride
    13811-627benazepril hydrochlorideBenazepril hydrochloride
    13811-628BENAZEPRIL HYDROCHLORIDEBenazepril hydrochloride
    13811-629BENAZEPRIL HYDROCHLORIDEBenazepril hydrochloride
    13811-630BENAZEPRIL HYDROCHLORIDEBenazepril hydrochloride
    21695-326Benazepril HydrochlorideBenazepril Hydrochloride
    21695-327Benazepril HydrochlorideBenazepril Hydrochloride
    21695-612Benazepril HydrochlorideBenazepril Hydrochloride
    21695-877Benazepril HydrochlorideBenazepril Hydrochloride
    23155-749Benazepril HydrochlorideBenazepril Hydrochloride
    23155-750Benazepril HydrochlorideBenazepril Hydrochloride
    23155-751Benazepril HydrochlorideBenazepril Hydrochloride
    23155-752Benazepril HydrochlorideBenazepril Hydrochloride
    33261-179Benazepril HydrochlorideBenazepril Hydrochloride
    33261-180Benazepril HydrochlorideBenazepril Hydrochloride
    33261-846Benazepril HydrochlorideBenazepril Hydrochloride
    42291-160Benazepril HydrochlorideBenazepril Hydrochloride
    42291-161Benazepril HydrochlorideBenazepril Hydrochloride
    42291-162Benazepril HydrochlorideBenazepril Hydrochloride
    68071-1146Benazepril HydrochlorideBenazepril Hydrochloride
    68071-1770Benazepril HydrochlorideBenazepril Hydrochloride
    68071-1026Benazepril HydrochlorideBenazepril Hydrochloride
    68071-3057Benazepril HydrochlorideBenazepril Hydrochloride
    68071-1969Benazepril HydrochlorideBenazepril Hydrochloride
    68071-3142Benazepril HydrochlorideBenazepril Hydrochloride
    68071-3324Benazepril HydrochlorideBenazepril Hydrochloride
    68071-4198Benazepril HydrochlorideBenazepril Hydrochloride
    68071-4722Benazepril HydrochlorideBenazepril Hydrochloride
    68382-169Benazepril hydrochlorideBenazepril hydrochloride
    68382-172Benazepril hydrochlorideBenazepril hydrochloride
    68382-171Benazepril hydrochlorideBenazepril hydrochloride
    68382-170Benazepril hydrochlorideBenazepril hydrochloride
    68788-6361Benazepril HydrochlorideBenazepril Hydrochloride
    68788-9313Benazepril HydrochlorideBenazepril Hydrochloride
    68788-7248Benazepril HydrochlorideBenazepril Hydrochloride
    68788-9052Benazepril HydrochlorideBenazepril Hydrochloride
    68788-6889Benazepril HydrochlorideBenazepril Hydrochloride
    68788-6957Benazepril HydrochlorideBenazepril Hydrochloride
    68788-8968Benazepril HydrochlorideBenazepril Hydrochloride
    68788-9947Benazepril HydrochlorideBenazepril Hydrochloride
    68788-9050Benazepril HydrochlorideBenazepril Hydrochloride
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