NDC 0469-0725

Xtandi

Enzalutamide

Xtandi is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Astellas Pharma Us, Inc.. The primary component is Enzalutamide.

Product ID0469-0725_25c3a7dd-b2f0-4188-a4c3-9ccc694ca7a9
NDC0469-0725
Product TypeHuman Prescription Drug
Proprietary NameXtandi
Generic NameEnzalutamide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2020-08-04
Marketing CategoryNDA / NDA
Application NumberNDA213674
Labeler NameAstellas Pharma US, Inc.
Substance NameENZALUTAMIDE
Active Ingredient Strength80 mg/1
Pharm ClassesAndrogen Receptor Inhibitor [EPC],Androgen Receptor Antagonists [MoA],Cytochrome P450 3A4 Inducers [MoA],Cytochrome P450 2C9 Inducers [MoA],Cytochrome P450 2C19 Inducers [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0469-0725-60

1 BOTTLE in 1 CARTON (0469-0725-60) > 60 TABLET in 1 BOTTLE
Marketing Start Date2020-08-04
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Xtandi" or generic name "Enzalutamide"

NDCBrand NameGeneric Name
0469-0125Xtandienzalutamide
0469-0625Xtandienzalutamide
0469-0725Xtandienzalutamide
0469-1125Xtandienzalutamide
0469-1725Xtandienzalutamide

Trademark Results [Xtandi]

Mark Image

Registration | Serial
Company
Trademark
Application Date
XTANDI
XTANDI
79110148 4181564 Live/Registered
Astellas Pharma Inc.
2011-12-27

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