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Quinapril

NDC 69097-839, Quinapril, tablet, from Cipla USA Inc..

Product NDC
69097-839
Status
Listed
Labeler
Cipla USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078457
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69097-839 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • QUINAPRIL HYDROCHLORIDE5 mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC]; Angiotensin-converting Enzyme Inhibitors [MoA]

Package NDCNDC-11Package
69097-839-056909708390590 TABLET in 1 BOTTLE (69097-839-05)
69097-839-15690970839151000 TABLET in 1 BOTTLE (69097-839-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e6d36e1e-8e35-4d06-83dc-45e0456365fd

Use it

Look up 69097-839 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-839 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-839. 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.