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Benazepril Hydrochloride and Hydrochlorothiazide

NDC 0185-0325, Benazepril Hydrochloride and Hydrochlorothiazide, tablet, film coated, from Sandoz Inc.

Product NDC
0185-0325
Status
Listed
Labeler
Sandoz Inc
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076631
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0185-0325 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BENAZEPRIL HYDROCHLORIDE10 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
0185-0325-0100185032501100 TABLET, FILM COATED in 1 BOTTLE (0185-0325-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c9bdfbb4-87b6-4de4-bc1d-5025d3ef591f

  • NADAC price for package 00185032501

    GET /v1/drugs/nadac/00185032501

Use it

Look up 0185-0325 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0185-0325 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0185-0325. 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.