NDC 50419-828

DESONATE

Desonide

DESONATE is a Topical Gel in the Human Prescription Drug category. It is labeled and distributed by Bayer Healthcare Pharmaceuticals Inc.. The primary component is Desonide.

Product ID50419-828_0e276ec9-8b14-4618-8219-5f3ad4bbc273
NDC50419-828
Product TypeHuman Prescription Drug
Proprietary NameDESONATE
Generic NameDesonide
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2006-10-20
Marketing CategoryNDA / NDA
Application NumberNDA021844
Labeler NameBayer HealthCare Pharmaceuticals Inc.
Substance NameDESONIDE
Active Ingredient Strength1 mg/g
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 50419-828-06

1 TUBE in 1 CARTON (50419-828-06) > 60 g in 1 TUBE
Marketing Start Date2019-07-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50419-828-72 [50419082872]

DESONATE GEL
Marketing CategoryNDA
Application NumberNDA021844
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-07-23

NDC 50419-828-12 [50419082812]

DESONATE GEL
Marketing CategoryNDA
Application NumberNDA021844
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date2019-07-23

NDC 50419-828-71 [50419082871]

DESONATE GEL
Marketing CategoryNDA
Application NumberNDA021844
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-10-20
Marketing End Date2014-08-06

NDC 50419-828-06 [50419082806]

DESONATE GEL
Marketing CategoryNDA
Application NumberNDA021844
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date2019-07-23

Drug Details

Active Ingredients

IngredientStrength
DESONIDE.5 mg/g

OpenFDA Data

SPL SET ID:8d7c46ed-e6c3-465b-be3d-16ecab43a9e7
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 669081
  • 692757
  • Pharmacological Class

    • Corticosteroid [EPC]
    • Corticosteroid Hormone Receptor Agonists [MoA]

    Medicade Reported Pricing

    50419082812 DESONATE 0.05% GEL

    Pricing Unit: GM | Drug Type:

    50419082806 DESONATE 0.05% GEL

    Pricing Unit: GM | Drug Type:

    NDC Crossover Matching brand name "DESONATE" or generic name "Desonide"

    NDCBrand NameGeneric Name
    10922-828DESONATEdesonide
    50222-504DESONATEdesonide
    50419-828DESONATEdesonide
    0115-1517DesonideDesonide
    0168-0309desonidedesonide
    0168-0310desonidedesonide
    0472-0803Desonidedesonide
    0472-0804Desonidedesonide
    0713-0661DesonideDesonide
    16714-729DesonideDesonide
    16714-828DesonideDesonide
    21695-944DESONIDEDESONIDE
    24470-920DESONIDEDesonide
    42254-142DesonideDesonide
    45802-422DesonideDesonide
    45802-423DesonideDesonide
    50436-3300DesonideDesonide
    51672-1280DesonideDesonide
    51672-1281DesonideDesonide
    51672-4079DesonideDesonide
    52187-556DESONIDEDESONIDE
    52565-038DesonideDesonide
    57893-317DESONIDEDesonide
    0299-5765DesOwendesonide
    0299-5770DesOwendesonide
    44118-710DESRXDESONIDE
    0462-0392LoKaradesonide
    16110-111Verdesodesonide

    Trademark Results [DESONATE]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    DESONATE
    DESONATE
    78356061 3276136 Live/Registered
    LEO PHARMA A/S
    2004-01-22
    DESONATE
    DESONATE
    77226193 3531883 Live/Registered
    LEO PHARMA A/S
    2007-07-10

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.