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Enalapril Maleate and Hydrochlorothiazide

NDC 51672-4045, Enalapril Maleate and Hydrochlorothiazide, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4045
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075788
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4045 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ENALAPRIL MALEATE5 mg/1
  • HYDROCHLOROTHIAZIDE12.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51672-4045-151672404501100 TABLET in 1 BOTTLE (51672-4045-1)
51672-4045-3516724045031000 TABLET in 1 BOTTLE (51672-4045-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7cb92cf2-46f2-4379-937c-168d230e43a4

  • NADAC price for package 51672404501

    GET /v1/drugs/nadac/51672404501

Use it

Look up 51672-4045 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4045 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4045. 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.