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HYDROXYCHLOROQUINE SULFATE

NDC 71610-701, HYDROXYCHLOROQUINE SULFATE, tablet, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-701
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210441
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-701 \
  -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
71610-701-537161007015360 TABLET in 1 BOTTLE (71610-701-53)
71610-701-8071610070180180 TABLET in 1 BOTTLE (71610-701-80)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/beff29fe-574f-4566-99ac-53ec3b3038a7

Use it

Look up 71610-701 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-701 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-701. 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.