lotensin

Generic: benazepril hydrochloride

Labeler: validus pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name lotensin
Generic Name benazepril hydrochloride
Labeler validus pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

benazepril hydrochloride 40 mg/1

Manufacturer
Validus Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 30698-450
Product ID 30698-450_40029d07-adfa-0cc3-e063-6294a90a4cd5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019851
Listing Expiration 2026-12-31
Marketing Start 1991-06-21

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 30698450
Hyphenated Format 30698-450

Supplemental Identifiers

RxCUI
898687 898689 898690 898692 898719 898721
UPC
0330698449011
UNII
N1SN99T69T

Packaging Origin

Original Packager
true

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 lotensin (source: ndc)
Generic Name benazepril hydrochloride (source: ndc)
Application Number NDA019851 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (30698-450-01)
source: ndc

Packages (1)

30698-450-01 100 TABLET in 1 BOTTLE (30698-450-01)

Ingredients (1)

benazepril hydrochloride (40 mg/1)

Linked Drug Pages (1)

Lotensin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40029d07-adfa-0cc3-e063-6294a90a4cd5", "openfda": {"upc": ["0330698449011"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898689", "898690", "898692", "898719", "898721"], "spl_set_id": ["2abb091b-a53e-46b0-9b84-e5ee8f2bdd8e"], "manufacturer_name": ["Validus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (30698-450-01)", "package_ndc": "30698-450-01", "marketing_start_date": "19910621"}], "brand_name": "Lotensin", "product_id": "30698-450_40029d07-adfa-0cc3-e063-6294a90a4cd5", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "30698-450", "generic_name": "benazepril hydrochloride", "labeler_name": "Validus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lotensin", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "NDA019851", "marketing_category": "NDA", "marketing_start_date": "19910621", "listing_expiration_date": "20261231"}