dapsone
Generic: dapsone
Labeler: avkareDrug Facts
Product Profile
Brand Name
dapsone
Generic Name
dapsone
Labeler
avkare
Dosage Form
TABLET
Routes
Active Ingredients
dapsone 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
73190-037
Product ID
73190-037_459c00ea-b9d0-85d0-e063-6294a90a166d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA086841
Listing Expiration
2026-12-31
Marketing Start
2025-12-10
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73190037
Hyphenated Format
73190-037
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA086841 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (73190-037-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "459c00ea-b9d0-85d0-e063-6294a90a166d", "openfda": {"nui": ["N0000175881", "M0020791"], "unii": ["8W5C518302"], "rxcui": ["197558"], "spl_set_id": ["459c00e0-2124-8965-e063-6294a90a4278"], "pharm_class_cs": ["Sulfones [CS]"], "pharm_class_epc": ["Sulfone [EPC]"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (73190-037-01)", "package_ndc": "73190-037-01", "marketing_start_date": "20251210"}], "brand_name": "Dapsone", "product_id": "73190-037_459c00ea-b9d0-85d0-e063-6294a90a166d", "dosage_form": "TABLET", "pharm_class": ["Sulfone [EPC]", "Sulfones [CS]"], "product_ndc": "73190-037", "generic_name": "Dapsone", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dapsone", "active_ingredients": [{"name": "DAPSONE", "strength": "25 mg/1"}], "application_number": "ANDA086841", "marketing_category": "ANDA", "marketing_start_date": "20251210", "listing_expiration_date": "20261231"}