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Hydroxychloroquine Sulfate

NDC 71610-961, Hydroxychloroquine Sulfate, tablet, film coated, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-961
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210577
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-961 \
  -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
71610-961-307161009613030 TABLET, FILM COATED in 1 BOTTLE (71610-961-30)
71610-961-537161009615360 TABLET, FILM COATED in 1 BOTTLE (71610-961-53)
71610-961-8071610096180180 TABLET, FILM COATED in 1 BOTTLE (71610-961-80)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/427ac2fc-8f7f-9725-e063-6394a90a381b

Use it

Look up 71610-961 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-961 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-961. 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.