amlodipine and benazepril hydrochloride
Generic: amlodipine and benazepril hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
amlodipine and benazepril hydrochloride
Generic Name
amlodipine and benazepril hydrochloride
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
amlodipine besylate 5 mg/1, benazepril hydrochloride 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0953
Product ID
71335-0953_3de54c49-3590-4a70-9268-fa68e434d923
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202239
Listing Expiration
2026-12-31
Marketing Start
2012-09-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350953
Hyphenated Format
71335-0953
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
amlodipine and benazepril hydrochloride (source: ndc)
Generic Name
amlodipine and benazepril hydrochloride (source: ndc)
Application Number
ANDA202239 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
- 20 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (71335-0953-1)
- 90 CAPSULE in 1 BOTTLE (71335-0953-2)
- 60 CAPSULE in 1 BOTTLE (71335-0953-3)
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3de54c49-3590-4a70-9268-fa68e434d923", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898356"], "spl_set_id": ["3de54c49-3590-4a70-9268-fa68e434d923"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-0953-1)", "package_ndc": "71335-0953-1", "marketing_start_date": "20180918"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71335-0953-2)", "package_ndc": "71335-0953-2", "marketing_start_date": "20191114"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71335-0953-3)", "package_ndc": "71335-0953-3", "marketing_start_date": "20240709"}], "brand_name": "Amlodipine and Benazepril Hydrochloride", "product_id": "71335-0953_3de54c49-3590-4a70-9268-fa68e434d923", "dosage_form": "CAPSULE", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Decreased Blood Pressure [PE]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "71335-0953", "generic_name": "Amlodipine and Benazepril Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA202239", "marketing_category": "ANDA", "marketing_start_date": "20120905", "listing_expiration_date": "20261231"}