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Fosinopril Sodium

NDC 65862-472, Fosinopril Sodium, tablet, from Aurobindo Pharma Limited.

Product NDC
65862-472
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091163
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-472 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FOSINOPRIL SODIUM20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
65862-472-306586204723030 TABLET in 1 BOTTLE (65862-472-30)
65862-472-906586204729090 TABLET in 1 BOTTLE (65862-472-90)
65862-472-99658620472991000 TABLET in 1 BOTTLE (65862-472-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/aee04f17-8ee9-42f5-861f-b6ba17220ca4

Use it

Look up 65862-472 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-472 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-472. 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.