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Benazepril Hydrochloride

NDC 43063-679, Benazepril Hydrochloride, tablet, coated, from PD-Rx Pharmaceuticals, Inc..

Product NDC
43063-679
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
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/43063-679 \
  -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
43063-679-304306306793030 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-679-30)
43063-679-904306306799090 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-679-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/355811f0-2885-0d49-e054-00144ff8d46c

Use it

Look up 43063-679 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43063-679 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43063-679. 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.