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Amiloride Hydrochloride

NDC 42794-005, Amiloride Hydrochloride, tablet, from Sigmapharm Laboratories, LLC.

Product NDC
42794-005
Status
Listed
Labeler
Sigmapharm Laboratories, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA079133
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42794-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMILORIDE HYDROCHLORIDE ANHYDROUS5 mg/1

Pharmacologic classes

Decreased Renal K+ Excretion [PE]; Increased Diuresis [PE]; Potassium-sparing Diuretic [EPC]

Package NDCNDC-11Package
42794-005-0242794000502100 TABLET in 1 BOTTLE (42794-005-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/de12b6f3-3791-4d78-90e6-c487cf951738

  • NADAC price for package 42794000502

    GET /v1/drugs/nadac/42794000502

Use it

Look up 42794-005 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42794-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42794-005. 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.