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Chlorthalidone

NDC 57664-649, Chlorthalidone, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
57664-649
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA089286
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57664-649 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CHLORTHALIDONE50 mg/1

Pharmacologic classes

Increased Diuresis [PE]; Thiazide-like Diuretic [EPC]

Package NDCNDC-11Package
57664-649-18576640649181000 TABLET in 1 BOTTLE (57664-649-18)
57664-649-8857664064988100 TABLET in 1 BOTTLE (57664-649-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a304de67-cd2b-4933-937e-4eeecf6cda40

  • NADAC price for package 57664064988

    GET /v1/drugs/nadac/57664064988

Use it

Look up 57664-649 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57664-649 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57664-649. 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.