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Enalapril Maleate

NDC 51672-4037, Enalapril Maleate, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4037
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075657
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4037 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ENALAPRIL MALEATE2.5 mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC]; Angiotensin-converting Enzyme Inhibitors [MoA]; Decreased Blood Pressure [PE]

Package NDCNDC-11Package
51672-4037-151672403701100 TABLET in 1 BOTTLE (51672-4037-1)
51672-4037-3516724037031000 TABLET in 1 BOTTLE (51672-4037-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f103b9f9-e081-419d-a2d8-b86acda834dd

  • NADAC price for package 51672403701

    GET /v1/drugs/nadac/51672403701

  • NADAC price for package 51672403703

    GET /v1/drugs/nadac/51672403703

Use it

Look up 51672-4037 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4037 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4037. 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.