NDC 59572-632

OTEZLA

Apremilast

OTEZLA is a Oral Kit in the Human Prescription Drug category. It is labeled and distributed by Celgene Corporation. The primary component is .

Product ID59572-632_4b03ba80-afc7-4904-8c87-ef84b8fd25ea
NDC59572-632
Product TypeHuman Prescription Drug
Proprietary NameOTEZLA
Generic NameApremilast
Dosage FormKit
Route of AdministrationORAL
Marketing Start Date2015-02-01
Marketing CategoryNDA / NDA
Application NumberNDA205437
Labeler NameCelgene Corporation
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 59572-632-55

1 KIT in 1 BLISTER PACK (59572-632-55)
Marketing Start Date2015-08-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 59572-632-55 [59572063255]

OTEZLA KIT
Marketing CategoryNDA
Application NumberNDA205437
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-08-05

Drug Details

OpenFDA Data

SPL SET ID:3acf6751-827d-11e2-9e96-0800200c9a66
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1605454
  • 1605455
  • 1492747
  • 1492746
  • 1492732
  • 1492744
  • 1492742
  • 1492740
  • 1492738
  • 1492748
  • UPC Code
  • 0359572631991
  • NDC Crossover Matching brand name "OTEZLA" or generic name "Apremilast"

    NDCBrand NameGeneric Name
    55513-137Otezlaapremilast
    55513-369Otezlaapremilast
    55513-485Otezlaapremilast
    59572-630OTEZLAapremilast
    59572-631OTEZLAapremilast
    59572-632OTEZLAapremilast
    70518-3155Otezlaapremilast
    60219-1410APREMILASTAPREMILAST
    60219-1744APREMILASTAPREMILAST

    Trademark Results [OTEZLA]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    OTEZLA
    OTEZLA
    86109590 4598910 Live/Registered
    Celgene Corporation
    2013-11-04
    OTEZLA
    OTEZLA
    86093816 4598865 Live/Registered
    Celgene Corporation
    2013-10-17
    OTEZLA
    OTEZLA
    85705380 4331247 Live/Registered
    Celgene Corporation
    2012-08-16

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