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Benazepril Hydrochloride

NDC 50090-3359, Benazepril Hydrochloride, tablet, film coated, from A-S Medication Solutions.

Product NDC
50090-3359
Status
Listed
Labeler
A-S Medication Solutions
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/50090-3359 \
  -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
50090-3359-05009033590030 TABLET, FILM COATED in 1 BOTTLE (50090-3359-0)
50090-3359-15009033590190 TABLET, FILM COATED in 1 BOTTLE (50090-3359-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c5090372-41bf-4677-b198-97fd55a0cb87

Use it

Look up 50090-3359 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-3359 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-3359. 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.