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Amiloride Hydrochloride and Hydrochlorothiazide

NDC 0555-0483, Amiloride Hydrochloride and Hydrochlorothiazide, tablet, from Teva Pharmaceuticals USA, Inc..

Product NDC
0555-0483
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA071111
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0555-0483 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMILORIDE HYDROCHLORIDE5 mg/1
  • HYDROCHLOROTHIAZIDE50 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0555-0483-0200555048302100 TABLET in 1 BOTTLE (0555-0483-02)
0555-0483-05005550483051000 TABLET in 1 BOTTLE (0555-0483-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8b2c581a-f955-4a8e-bf85-e768e903fd10

  • NADAC price for package 00555048302

    GET /v1/drugs/nadac/00555048302

  • NADAC price for package 00555048305

    GET /v1/drugs/nadac/00555048305

Use it

Look up 0555-0483 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0555-0483 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0555-0483. 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.