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Fosinopril Sodium and Hydrochlorothiazide

NDC 69097-972, Fosinopril Sodium and Hydrochlorothiazide, tablet, from CIPLA USA INC..

Product NDC
69097-972
Status
Listed
Labeler
CIPLA USA INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090228
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69097-972 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FOSINOPRIL SODIUM10 mg/1
  • HYDROCHLOROTHIAZIDE12.5 mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC]; Angiotensin-converting Enzyme Inhibitors [MoA]; Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]

Package NDCNDC-11Package
69097-972-0769097097207100 TABLET in 1 BOTTLE (69097-972-07)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4e1ed7da-029e-48d6-a5e4-fc7ac11192fb

  • NADAC price for package 69097097207

    GET /v1/drugs/nadac/69097097207

Use it

Look up 69097-972 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-972 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-972. 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.