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HYDROXYCHLOROQUINE SULFATE

NDC 82619-131, hydroxychloroquine sulfate, tablet, from Creekwood Pharmaceuticals LLC.

Product NDC
82619-131
Status
Listed
Labeler
Creekwood Pharmaceuticals LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040150
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82619-131 \
  -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
82619-131-0182619013101100 TABLET in 1 BOTTLE (82619-131-01)
82619-131-0282619013102500 TABLET in 1 BOTTLE (82619-131-02)
82619-131-03826190131031000 TABLET in 1 BOTTLE (82619-131-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/04139607-f7c0-4fe1-a210-ffa5af347d56

Use it

Look up 82619-131 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82619-131 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82619-131. 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.