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Hydroxychloroquine sulfate

NDC 16714-110, Hydroxychloroquine sulfate, tablet, film coated, from Northstar Rx LLC..

Product NDC
16714-110
Status
Listed
Labeler
Northstar Rx LLC.
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/16714-110 \
  -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
16714-110-0116714011001100 TABLET, FILM COATED in 1 BOTTLE (16714-110-01)
16714-110-0216714011002500 TABLET, FILM COATED in 1 BOTTLE (16714-110-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/29ba0172-7ca3-4122-af1b-f0da522318cb

  • NADAC price for package 16714011001

    GET /v1/drugs/nadac/16714011001

  • NADAC price for package 16714011002

    GET /v1/drugs/nadac/16714011002

Use it

Look up 16714-110 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-110 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-110. 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.