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Hydroxychloroquine sulfate

NDC 57664-761, Hydroxychloroquine sulfate, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
57664-761
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201691
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57664-761 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROXYCHLOROQUINE SULFATE200 mg/1

Pharmacologic classes

Antimalarial [EPC]; Antirheumatic Agent [EPC]

Package NDCNDC-11Package
57664-761-1357664076113500 TABLET in 1 BOTTLE (57664-761-13)
57664-761-8857664076188100 TABLET in 1 BOTTLE (57664-761-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6e72fe06-7995-3fd7-e053-2a91aa0a54db

Use it

Look up 57664-761 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57664-761 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57664-761. 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.