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Hydroxychloroquine Sulfate

NDC 60219-1544, Hydroxychloroquine Sulfate, tablet, film coated, from Amneal Pharmaceuticals NY LLC.

Product NDC
60219-1544
Status
Listed
Labeler
Amneal Pharmaceuticals NY 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/60219-1544 \
  -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
60219-1544-160219154401100 TABLET, FILM COATED in 1 BOTTLE (60219-1544-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6a9e2fc8-bedf-46d4-9973-328dbcb18061

Use it

Look up 60219-1544 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60219-1544 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60219-1544. 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.