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BENAZEPRIL HYDROCHLORIDE

NDC 72189-110, BENAZEPRIL HYDROCHLORIDE, tablet, coated, from DIRECT RX.

Product NDC
72189-110
Status
Listed
Labeler
DIRECT RX
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076118
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-110 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BENAZEPRIL HYDROCHLORIDE10 mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC]; Angiotensin-converting Enzyme Inhibitors [MoA]; Decreased Blood Pressure [PE]

Package NDCNDC-11Package
72189-110-307218901103030 TABLET, COATED in 1 BOTTLE (72189-110-30)
72189-110-907218901109090 TABLET, COATED in 1 BOTTLE (72189-110-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a7e4e43a-7abc-e2a5-e053-2995a90ab5f4

Use it

Look up 72189-110 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-110 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-110. 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.