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HYDROXYCHLOROQUINE SULFATE

NDC 43598-131, HYDROXYCHLOROQUINE SULFATE, tablet, film coated, from Dr. Reddy's Laboratories Inc..

Product NDC
43598-131
Status
Listed
Labeler
Dr. Reddy's Laboratories Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210441
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43598-131 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROXYCHLOROQUINE SULFATE400 mg/1

Pharmacologic classes

Antimalarial [EPC]; Antirheumatic Agent [EPC]

Package NDCNDC-11Package
43598-131-0143598013101100 TABLET, FILM COATED in 1 BOTTLE (43598-131-01)
43598-131-0543598013105500 TABLET, FILM COATED in 1 BOTTLE (43598-131-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/452092b4-7a8f-4d19-8113-f1c2a948d3d8

  • NADAC price for package 43598013101

    GET /v1/drugs/nadac/43598013101

Use it

Look up 43598-131 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43598-131 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43598-131. 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.