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
33342-535_839d7440-ba0e-4c56-b648-d374b155cf03
Product NDC
33342-535
Form
TABLET
Composition / generic term
Dapsone
Labeler
Macleods Pharmaceuticals Limited
Marketing category
ANDA
Marketing start / end (source format)
20260708
Source listing expiry
20271231

Source-listed ingredients

  • DAPSONE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (33342-535-07) · 33342-535-07
  • 100 TABLET in 1 BOTTLE (33342-535-11) · 33342-535-11

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.

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