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Amiloride Hydrochloride

NDC 49884-117, Amiloride Hydrochloride, tablet, from Par Health USA, LLC.

Product NDC
49884-117
Status
Listed
Labeler
Par Health USA, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA070346
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/49884-117 \
  -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
49884-117-0149884011701100 TABLET in 1 BOTTLE (49884-117-01)
49884-117-10498840117101000 TABLET in 1 BOTTLE (49884-117-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e0cc2d44-436a-47e8-a890-589882fff4c4

  • NADAC price for package 49884011701

    GET /v1/drugs/nadac/49884011701

  • NADAC price for package 49884011710

    GET /v1/drugs/nadac/49884011710

Use it

Look up 49884-117 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49884-117 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49884-117. 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.