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Benazepril Hydrochloride

NDC 62559-526, Benazepril Hydrochloride, tablet, from ANI Pharmaceuticals, Inc..

Product NDC
62559-526
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076333
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62559-526 \
  -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
62559-526-0162559052601100 TABLET in 1 BOTTLE (62559-526-01)
62559-526-0562559052605500 TABLET in 1 BOTTLE (62559-526-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ff732cfa-9ded-4226-b464-19c90a6865ae

Use it

Look up 62559-526 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62559-526 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62559-526. 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.