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amiloride hydrochloride

NDC 0574-0292, amiloride hydrochloride, tablet, from Padagis US LLC.

Product NDC
0574-0292
Status
Listed
Labeler
Padagis US LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA018200
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0574-0292 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMILORIDE HYDROCHLORIDE5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0574-0292-0100574029201100 TABLET in 1 BOTTLE (0574-0292-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2b70cf0c-45be-428f-b396-5001ed4e30fc
  • NADAC price for package 00574029201

    GET /v1/drugs/nadac/00574029201

Use it

Look up 0574-0292 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0574-0292 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0574-0292. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.