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Benazepril Hydrochloride

NDC 51655-202, Benazepril Hydrochloride, tablet, film coated, from Northwind Health Company, LLC.

Product NDC
51655-202
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078212
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-202 \
  -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
51655-202-265165502022690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-202-26)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f7f9dc46-a947-7ae3-e053-6394a90a1192

Use it

Look up 51655-202 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-202 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-202. 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.