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Fosinopril Sodium

NDC 69097-856, Fosinopril, tablet, from Cipla USA Inc..

Product NDC
69097-856
Status
Listed
Labeler
Cipla USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077222
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69097-856 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FOSINOPRIL SODIUM10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
69097-856-056909708560590 TABLET in 1 BOTTLE (69097-856-05)
69097-856-15690970856151000 TABLET in 1 BOTTLE (69097-856-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/736fe52f-69fb-48b2-b1c5-f06531878538

  • NADAC price for package 69097085605

    GET /v1/drugs/nadac/69097085605

Use it

Look up 69097-856 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-856 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-856. 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.