desonide

Generic: desonide

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desonide
Generic Name desonide
Labeler actavis pharma, inc.
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

desonide .5 mg/mL

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0472-0803
Product ID 0472-0803_f3953b9e-138f-4d86-8eea-0fc03c3c2747
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072354
Marketing Start 2009-05-28
Marketing End 2028-03-31

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04720803
Hyphenated Format 0472-0803

Supplemental Identifiers

RxCUI
197572 349351
UPC
0304720804604 0304720803041
UNII
J280872D1O
NUI
N0000175576 N0000175450

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 desonide (source: ndc)
Generic Name desonide (source: ndc)
Application Number ANDA072354 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0472-0803-02) / 59 mL in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0472-0803-04) / 118 mL in 1 BOTTLE
source: ndc

Packages (2)

Ingredients (1)

desonide (.5 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "f3953b9e-138f-4d86-8eea-0fc03c3c2747", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0304720804604", "0304720803041"], "unii": ["J280872D1O"], "rxcui": ["197572", "349351"], "spl_set_id": ["ff5d4cd8-ab4d-4a9e-b84b-445c81eeea99"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0472-0803-02)  / 59 mL in 1 BOTTLE", "package_ndc": "0472-0803-02", "marketing_end_date": "20270228", "marketing_start_date": "20090528"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0472-0803-04)  / 118 mL in 1 BOTTLE", "package_ndc": "0472-0803-04", "marketing_end_date": "20280331", "marketing_start_date": "20090528"}], "brand_name": "Desonide", "product_id": "0472-0803_f3953b9e-138f-4d86-8eea-0fc03c3c2747", "dosage_form": "LOTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0472-0803", "generic_name": "desonide", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desonide", "active_ingredients": [{"name": "DESONIDE", "strength": ".5 mg/mL"}], "application_number": "ANDA072354", "marketing_category": "ANDA", "marketing_end_date": "20280331", "marketing_start_date": "20090528"}