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Chlorothiazide Sodium

NDC 0517-1820, Chlorothiazide Sodium, injection, powder, lyophilized, for solution, from American Regent, Inc..

Product NDC
0517-1820
Status
Listed
Labeler
American Regent, Inc.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202561
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0517-1820 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CHLOROTHIAZIDE SODIUM500 mg/18mL

Pharmacologic classes

Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]

Package NDCNDC-11Package
0517-1820-01005171820011 VIAL in 1 CARTON (0517-1820-01) / 18 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/850960a3-9fe2-4999-81eb-b0ae9ba011bc

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0517-1820

Use it

Look up 0517-1820 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0517-1820 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0517-1820. 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.