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DAPSONE

NDC 60758-670, dapsone, gel, from Pacific Pharma, Inc..

Product NDC
60758-670
Status
Listed
Labeler
Pacific Pharma, Inc.
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA021794
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60758-670 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DAPSONE50 mg/g

Pharmacologic classes

Sulfone [EPC]; Sulfones [CS]

Package NDCNDC-11Package
60758-670-30607580670301 TUBE in 1 CARTON (60758-670-30) / 30 g in 1 TUBE
60758-670-60607580670601 TUBE in 1 CARTON (60758-670-60) / 60 g in 1 TUBE
60758-670-90607580670901 TUBE in 1 CARTON (60758-670-90) / 90 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8dbe1a41-6d9d-414f-aa9c-09bd95857e2a

Use it

Look up 60758-670 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60758-670 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60758-670. 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.