benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

benazepril hydrochloride 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3243
Product ID 50090-3243_fdee60ff-213d-4b76-8c7b-952cbb037ad9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076118
Listing Expiration 2027-12-31
Marketing Start 2014-01-01

Pharmacologic Class

Classes
angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa] decreased blood pressure [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500903243
Hyphenated Format 50090-3243

Supplemental Identifiers

RxCUI
898690
UNII
N1SN99T69T

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, COATED in 1 BOTTLE (50090-3243-0)
  • 90 TABLET, COATED in 1 BOTTLE (50090-3243-1)
source: ndc

Packages (2)

50090-3243-0 30 TABLET, COATED in 1 BOTTLE (50090-3243-0) 50090-3243-1 90 TABLET, COATED in 1 BOTTLE (50090-3243-1)

Ingredients (1)

benazepril hydrochloride (20 mg/1)

Linked Drug Pages (1)

Benazepril Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fdee60ff-213d-4b76-8c7b-952cbb037ad9", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898690"], "spl_set_id": ["7aac6a2f-85fb-4c7a-b424-9c253186dffe"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (50090-3243-0)", "package_ndc": "50090-3243-0", "marketing_start_date": "20171117"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (50090-3243-1)", "package_ndc": "50090-3243-1", "marketing_start_date": "20171103"}], "brand_name": "Benazepril Hydrochloride", "product_id": "50090-3243_fdee60ff-213d-4b76-8c7b-952cbb037ad9", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "50090-3243", "generic_name": "Benazepril Hydrochloride", "labeler_name": "A-S Medication Solutions", "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": "20271231"}