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Benazepril Hydrochloride

NDC 70518-2125, Benazepril Hydrochloride, tablet, coated, from REMEDYREPACK INC..

Product NDC
70518-2125
Status
Listed
Labeler
REMEDYREPACK 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/70518-2125 \
  -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
70518-2125-07051821250090 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2125-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/afd616b9-0c75-48be-862d-5ac18364fd9d

Use it

Look up 70518-2125 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2125 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-2125. 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.