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Benazepril Hydrochloride

NDC 71205-320, Benazepril Hydrochloride, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-320
Status
Listed
Labeler
Proficient Rx LP
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/71205-320 \
  -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
71205-320-307120503203030 TABLET, FILM COATED in 1 BOTTLE (71205-320-30)
71205-320-607120503206060 TABLET, FILM COATED in 1 BOTTLE (71205-320-60)
71205-320-907120503209090 TABLET, FILM COATED in 1 BOTTLE (71205-320-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/92a26516-3d84-4d7a-a770-523926507887

Use it

Look up 71205-320 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-320 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-320. 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.