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HYDROXYCHLOROQUINE SULFATE

NDC 42385-971, HYDROXYCHLOROQUINE SULFATE, tablet, film coated, from Laurus Labs Limited.

Product NDC
42385-971
Status
Listed
Labeler
Laurus Labs Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210959
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42385-971 \
  -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
42385-971-0142385097101100 TABLET, FILM COATED in 1 BOTTLE (42385-971-01)
42385-971-0542385097105500 TABLET, FILM COATED in 1 BOTTLE (42385-971-05)
42385-971-11423850971111000 TABLET, FILM COATED in 1 BOTTLE (42385-971-11)
42385-971-604238509716060 TABLET, FILM COATED in 1 BOTTLE (42385-971-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/04d8fdbf-8829-4469-a341-8af2a2d91ccc

Use it

Look up 42385-971 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42385-971 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42385-971. 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.