naftin
Generic: naftifine hydrochloride
Labeler: legacy pharma usa inc.Drug Facts
Product Profile
Brand Name
naftin
Generic Name
naftifine hydrochloride
Labeler
legacy pharma usa inc.
Dosage Form
GEL
Routes
Active Ingredients
naftifine hydrochloride 2 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
83107-023
Product ID
83107-023_3b299c91-fdf6-726c-e063-6394a90ad77b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA204286
Listing Expiration
2026-12-31
Marketing Start
2025-07-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83107023
Hyphenated Format
83107-023
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
naftin (source: ndc)
Generic Name
naftifine hydrochloride (source: ndc)
Application Number
NDA204286 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 g/100g
Packaging
- 1 TUBE in 1 CARTON (83107-023-45) / 45 g in 1 TUBE
- 1 TUBE in 1 CARTON (83107-023-60) / 60 g in 1 TUBE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3b299c91-fdf6-726c-e063-6394a90ad77b", "openfda": {"upc": ["0383107023609"], "unii": ["25UR9N9041"], "rxcui": ["1433734", "1433736"], "spl_set_id": ["6c6ee055-4031-45a7-8561-ccd989343580"], "manufacturer_name": ["Legacy Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (83107-023-45) / 45 g in 1 TUBE", "package_ndc": "83107-023-45", "marketing_start_date": "20250729"}, {"sample": false, "description": "1 TUBE in 1 CARTON (83107-023-60) / 60 g in 1 TUBE", "package_ndc": "83107-023-60", "marketing_start_date": "20250729"}], "brand_name": "Naftin", "product_id": "83107-023_3b299c91-fdf6-726c-e063-6394a90ad77b", "dosage_form": "GEL", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "83107-023", "generic_name": "Naftifine Hydrochloride", "labeler_name": "Legacy Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naftin", "active_ingredients": [{"name": "NAFTIFINE HYDROCHLORIDE", "strength": "2 g/100g"}], "application_number": "NDA204286", "marketing_category": "NDA", "marketing_start_date": "20250729", "listing_expiration_date": "20261231"}