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Hydroxychloroquine sulfate

NDC 68788-7747, Hydroxychloroquine sulfate, tablet, film coated, from Preferred Pharmaceuticals, Inc..

Product NDC
68788-7747
Status
Listed
Labeler
Preferred Pharmaceuticals, 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/68788-7747 \
  -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
68788-7747-26878877470220 TABLET, FILM COATED in 1 BOTTLE (68788-7747-2)
68788-7747-36878877470330 TABLET, FILM COATED in 1 BOTTLE (68788-7747-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d6c8ee2e-116e-4167-8d1a-bd570a1ce672

Use it

Look up 68788-7747 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7747 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-7747. 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.