United States · FDA National Drug Code directory
DAPSONE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 60758-670_41079403-219e-4194-90e8-3b9b83dcf298
- Product NDC
- 60758-670
- Form
- GEL
- Composition / generic term
- dapsone
- Labeler
- Pacific Pharma, Inc.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20171018
- Source listing expiry
- 20261231
Source-listed ingredients
- DAPSONE — 50 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (60758-670-30) / 30 g in 1 TUBE · 60758-670-30
- 1 TUBE in 1 CARTON (60758-670-60) / 60 g in 1 TUBE · 60758-670-60
- 1 TUBE in 1 CARTON (60758-670-90) / 90 g in 1 TUBE · 60758-670-90
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →