NDC 70771-1150

Benazepril hydrochloride

Benazepril Hydrochloride

Benazepril hydrochloride is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Cadila Healthcare Limited. The primary component is Benazepril Hydrochloride.

Product ID70771-1150_21dc4d8a-fb9e-46ec-b456-159551ff8d49
NDC70771-1150
Product TypeHuman Prescription Drug
Proprietary NameBenazepril hydrochloride
Generic NameBenazepril Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-11-13
Marketing CategoryANDA / ANDA
Application NumberANDA078848
Labeler NameCadila Healthcare Limited
Substance NameBENAZEPRIL HYDROCHLORIDE
Active Ingredient Strength20 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 70771-1150-0

1000 TABLET, FILM COATED in 1 BOTTLE (70771-1150-0)
Marketing Start Date2017-11-13
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70771-1150-2 [70771115002]

Benazepril hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078848
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-11-13

NDC 70771-1150-4 [70771115004]

Benazepril hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078848
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-11-13

NDC 70771-1150-9 [70771115009]

Benazepril hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078848
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-11-13

NDC 70771-1150-0 [70771115000]

Benazepril hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078848
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-11-13

NDC 70771-1150-1 [70771115001]

Benazepril hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078848
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-11-13

Drug Details

Active Ingredients

IngredientStrength
BENAZEPRIL HYDROCHLORIDE20 mg/1

OpenFDA Data

SPL SET ID:2e04ce38-7f44-49d1-9471-a0141631594e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 898690
  • 898719
  • 898687
  • 898723
  • 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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.