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Hydroxychloroquine sulfate

NDC 65841-633, Hydroxychloroquine sulfate, tablet, film coated, from Zydus Lifesciences Limited.

Product NDC
65841-633
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040657
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65841-633 \
  -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
65841-633-0165841063301100 TABLET, FILM COATED in 1 BOTTLE (65841-633-01)
65841-633-0565841063305500 TABLET, FILM COATED in 1 BOTTLE (65841-633-05)
65841-633-306584106333010 BLISTER PACK in 1 CARTON (65841-633-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1aa44bff-9a62-48b4-a520-98d7d524e3a9

Use it

Look up 65841-633 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65841-633 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65841-633. 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.