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Benazepril Hydrochloride

NDC 68071-1769, Benazepril Hydrochloride, tablet, coated, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-1769
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
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/68071-1769 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BENAZEPRIL HYDROCHLORIDE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68071-1769-168071176901100 TABLET, COATED in 1 BOTTLE (68071-1769-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9535ec77-2d50-4817-e053-2995a90a007e

Use it

Look up 68071-1769 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-1769 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-1769. 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.