desonide
Generic: desonide
Labeler: advanced rx of tennessee, llcDrug Facts
Product Profile
Brand Name
desonide
Generic Name
desonide
Labeler
advanced rx of tennessee, llc
Dosage Form
CREAM
Routes
Active Ingredients
desonide .5 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
80425-0418
Product ID
80425-0418_1d76541f-80d7-2a55-e063-6294a90aa5f9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074027
Listing Expiration
2026-12-31
Marketing Start
2024-07-17
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
804250418
Hyphenated Format
80425-0418
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
desonide (source: ndc)
Generic Name
desonide (source: ndc)
Application Number
ANDA074027 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/g
Packaging
- 1 TUBE in 1 CARTON (80425-0418-1) / 60 g in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1d76541f-80d7-2a55-e063-6294a90aa5f9", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["J280872D1O"], "rxcui": ["349351"], "spl_set_id": ["1d7632a7-0f27-9e5d-e063-6294a90ad21f"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (80425-0418-1) / 60 g in 1 TUBE", "package_ndc": "80425-0418-1", "marketing_start_date": "20240717"}], "brand_name": "Desonide", "product_id": "80425-0418_1d76541f-80d7-2a55-e063-6294a90aa5f9", "dosage_form": "CREAM", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "80425-0418", "generic_name": "Desonide", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desonide", "active_ingredients": [{"name": "DESONIDE", "strength": ".5 mg/g"}], "application_number": "ANDA074027", "marketing_category": "ANDA", "marketing_start_date": "20240717", "listing_expiration_date": "20261231"}