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Benazepril Hydrochloride

NDC 51655-066, Benazepril Hydrochloride, tablet, coated, from Northwind Health Company, LLC.

Product NDC
51655-066
Status
Listed
Labeler
Northwind Health Company, LLC
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/51655-066 \
  -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
51655-066-265165500662690 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-066-26)
51655-066-525165500665230 TABLET, COATED in 1 BOTTLE, DISPENSING (51655-066-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/708110e5-fa45-44e0-9011-261f4490ea45

Use it

Look up 51655-066 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-066 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-066. 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.