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Benazepril Hydrochloride

NDC 65862-118, Benazepril Hydrochloride, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-118
Status
Listed
Labeler
Aurobindo Pharma Limited
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/65862-118 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BENAZEPRIL HYDROCHLORIDE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
65862-118-0165862011801100 TABLET, FILM COATED in 1 BOTTLE (65862-118-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/09e383a8-e912-4cf7-8fb3-05545af80dd0

  • NADAC price for package 65862011801

    GET /v1/drugs/nadac/65862011801

Use it

Look up 65862-118 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-118 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-118. 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.