benazepril hydrochloride
Generic: benazepril hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
benazepril hydrochloride
Generic Name
benazepril hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET, COATED
Routes
Active Ingredients
benazepril hydrochloride 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0078
Product ID
71335-0078_c561231e-6648-43dc-a435-ac40c8b4cc1f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076118
Listing Expiration
2026-12-31
Marketing Start
2014-01-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350078
Hyphenated Format
71335-0078
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
benazepril hydrochloride (source: ndc)
Generic Name
benazepril hydrochloride (source: ndc)
Application Number
ANDA076118 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 TABLET, COATED in 1 BOTTLE (71335-0078-1)
- 60 TABLET, COATED in 1 BOTTLE (71335-0078-2)
- 100 TABLET, COATED in 1 BOTTLE (71335-0078-3)
- 90 TABLET, COATED in 1 BOTTLE (71335-0078-4)
- 14 TABLET, COATED in 1 BOTTLE (71335-0078-5)
- 10 TABLET, COATED in 1 BOTTLE (71335-0078-6)
Packages (6)
71335-0078-1
30 TABLET, COATED in 1 BOTTLE (71335-0078-1)
71335-0078-2
60 TABLET, COATED in 1 BOTTLE (71335-0078-2)
71335-0078-3
100 TABLET, COATED in 1 BOTTLE (71335-0078-3)
71335-0078-4
90 TABLET, COATED in 1 BOTTLE (71335-0078-4)
71335-0078-5
14 TABLET, COATED in 1 BOTTLE (71335-0078-5)
71335-0078-6
10 TABLET, COATED in 1 BOTTLE (71335-0078-6)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c561231e-6648-43dc-a435-ac40c8b4cc1f", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898690"], "spl_set_id": ["0653322d-70c6-45f7-a9d1-41efee1d7387"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (71335-0078-1)", "package_ndc": "71335-0078-1", "marketing_start_date": "20220209"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (71335-0078-2)", "package_ndc": "71335-0078-2", "marketing_start_date": "20220209"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (71335-0078-3)", "package_ndc": "71335-0078-3", "marketing_start_date": "20220209"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71335-0078-4)", "package_ndc": "71335-0078-4", "marketing_start_date": "20220209"}, {"sample": false, "description": "14 TABLET, COATED in 1 BOTTLE (71335-0078-5)", "package_ndc": "71335-0078-5", "marketing_start_date": "20220209"}, {"sample": false, "description": "10 TABLET, COATED in 1 BOTTLE (71335-0078-6)", "package_ndc": "71335-0078-6", "marketing_start_date": "20220209"}], "brand_name": "Benazepril Hydrochloride", "product_id": "71335-0078_c561231e-6648-43dc-a435-ac40c8b4cc1f", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71335-0078", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}