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Dapsone

NDC 51672-4197, Dapsone, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4197
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209430
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4197 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DAPSONE25 mg/1

Pharmacologic classes

Sulfone [EPC]; Sulfones [CS]

Package NDCNDC-11Package
51672-4197-65167241970630 TABLET in 1 BOTTLE (51672-4197-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cb312185-b9f1-4fa4-9481-bcf5d9bb3edf

Use it

Look up 51672-4197 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4197 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4197. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.