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Hydroxychloroquine sulfate

NDC 76420-850, Hydroxychloroquine sulfate, tablet, film coated, from Asclemed USA, Inc..

Product NDC
76420-850
Status
Listed
Labeler
Asclemed USA, Inc.
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/76420-850 \
  -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
76420-850-0176420085001100 TABLET, FILM COATED in 1 BOTTLE (76420-850-01)
76420-850-0576420085005500 TABLET, FILM COATED in 1 BOTTLE (76420-850-05)
76420-850-307642008503030 TABLET, FILM COATED in 1 BOTTLE (76420-850-30)
76420-850-607642008506060 TABLET, FILM COATED in 1 BOTTLE (76420-850-60)
76420-850-907642008509090 TABLET, FILM COATED in 1 BOTTLE (76420-850-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/19816051-c25e-44b5-a127-e846dbd0a8d8

Use it

Look up 76420-850 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-850 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-850. 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.