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benazepril hydrochloride and hydrochlorothiazide

NDC 72162-2328, benazepril hydrochloride and hydrochlorothiazide, tablet, from Bryant Ranch Prepack.

Product NDC
72162-2328
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA020033
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2328 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BENAZEPRIL HYDROCHLORIDE20 mg/1
  • HYDROCHLOROTHIAZIDE12.5 mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC]; Angiotensin-converting Enzyme Inhibitors [MoA]; Decreased Blood Pressure [PE]; Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]

Package NDCNDC-11Package
72162-2328-172162232801100 TABLET in 1 BOTTLE (72162-2328-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f4120568-dd9b-47a5-bd44-4de6ed343bbe

Use it

Look up 72162-2328 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2328 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-2328. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.