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HYDROXYCHLOROQUINE SULFATE

NDC 59651-889, HYDROXYCHLOROQUINE SULFATE, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
59651-889
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040274
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-889 \
  -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
59651-889-0159651088901100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59651-889-01)
59651-889-0559651088905500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59651-889-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e6f889ff-c5ba-4324-b87c-ec3ac942be2f

  • NADAC price for package 59651088901

    GET /v1/drugs/nadac/59651088901

  • NADAC price for package 59651088905

    GET /v1/drugs/nadac/59651088905

Use it

Look up 59651-889 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-889 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-889. 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.