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Lotensin

NDC 30698-449, benazepril hydrochloride, tablet, from Validus Pharmaceuticals LLC.

Product NDC
30698-449
Status
Listed
Labeler
Validus Pharmaceuticals LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA019851
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/30698-449 \
  -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
30698-449-0130698044901100 TABLET in 1 BOTTLE (30698-449-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2abb091b-a53e-46b0-9b84-e5ee8f2bdd8e

Use it

Look up 30698-449 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/30698-449 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 30698-449. 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.