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HYDROXYCHLOROQUINE SULFATE

NDC 71335-2813, hydroxychloroquine sulfate, tablet, from Bryant Ranch Prepack.

Product NDC
71335-2813
Status
Listed
Labeler
Bryant Ranch Prepack
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/71335-2813 \
  -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
71335-2813-171335281301100 TABLET in 1 BOTTLE (71335-2813-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f95cfc03-5023-44b3-8994-25afac18b734

Use it

Look up 71335-2813 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2813 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2813. 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.