NDC 71335-1086

Benazepril Hydrochloride

Benazepril Hydrochloride

Benazepril Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Benazepril Hydrochloride.

Product ID71335-1086_48abb287-11d9-4444-98b0-919b673c37f8
NDC71335-1086
Product TypeHuman Prescription Drug
Proprietary NameBenazepril Hydrochloride
Generic NameBenazepril Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2010-02-02
Marketing CategoryANDA / ANDA
Application NumberANDA076820
Labeler NameBryant Ranch Prepack
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 Through2020-12-31

Packaging

NDC 71335-1086-1

30 TABLET in 1 BOTTLE (71335-1086-1)
Marketing Start Date2010-07-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-1086-5 [71335108605]

Benazepril Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076820
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-07-21
Marketing End Date2019-09-12

NDC 71335-1086-3 [71335108603]

Benazepril Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076820
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-07-21
Marketing End Date2019-09-12

NDC 71335-1086-6 [71335108606]

Benazepril Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076820
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-07-21
Marketing End Date2019-09-12

NDC 71335-1086-4 [71335108604]

Benazepril Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076820
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-07-21
Marketing End Date2019-09-12

NDC 71335-1086-2 [71335108602]

Benazepril Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076820
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-07-21
Marketing End Date2019-09-12

NDC 71335-1086-1 [71335108601]

Benazepril Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076820
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-07-21
Marketing End Date2019-09-12

Drug Details

Active Ingredients

IngredientStrength
BENAZEPRIL HYDROCHLORIDE20 mg/1

OpenFDA Data

SPL SET ID:cd1a7c8f-cc61-4ee4-a259-0b3329cced3e
Manufacturer
UNII

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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