dapsone

Generic: dapsone

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dapsone
Generic Name dapsone
Labeler westminster pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dapsone 100 mg/1

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-410
Product ID 69367-410_94a7ec84-91fc-4cb2-9ddc-49e82e94408f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA086842
Listing Expiration 2026-12-31
Marketing Start 2025-08-21

Pharmacologic Class

Established (EPC)
sulfone [epc]
Chemical Structure
sulfones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69367410
Hyphenated Format 69367-410

Supplemental Identifiers

RxCUI
197557 197558
UPC
0369367410304 0369367409308
UNII
8W5C518302
NUI
N0000175881 M0020791

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name dapsone (source: ndc)
Generic Name dapsone (source: ndc)
Application Number ANDA086842 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69367-410-01)
  • 30 TABLET in 1 BOTTLE (69367-410-30)
source: ndc

Packages (2)

69367-410-01 100 TABLET in 1 BOTTLE (69367-410-01) 69367-410-30 30 TABLET in 1 BOTTLE (69367-410-30)

Ingredients (1)

dapsone (100 mg/1)

Linked Drug Pages (1)

Dapsone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "94a7ec84-91fc-4cb2-9ddc-49e82e94408f", "openfda": {"nui": ["N0000175881", "M0020791"], "upc": ["0369367410304", "0369367409308"], "unii": ["8W5C518302"], "rxcui": ["197557", "197558"], "spl_set_id": ["7d317576-5edd-4c27-a00d-68b5944c04a8"], "pharm_class_cs": ["Sulfones [CS]"], "pharm_class_epc": ["Sulfone [EPC]"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69367-410-01)", "package_ndc": "69367-410-01", "marketing_start_date": "20250821"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (69367-410-30)", "package_ndc": "69367-410-30", "marketing_start_date": "20250821"}], "brand_name": "Dapsone", "product_id": "69367-410_94a7ec84-91fc-4cb2-9ddc-49e82e94408f", "dosage_form": "TABLET", "pharm_class": ["Sulfone [EPC]", "Sulfones [CS]"], "product_ndc": "69367-410", "generic_name": "Dapsone", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dapsone", "active_ingredients": [{"name": "DAPSONE", "strength": "100 mg/1"}], "application_number": "ANDA086842", "marketing_category": "ANDA", "marketing_start_date": "20250821", "listing_expiration_date": "20261231"}