NDC 66993-212

Nilutamide

Nilutamide

Nilutamide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Prasco Laboratories. The primary component is Nilutamide.

Product ID66993-212_827f3aa0-e545-4678-be80-1a2d492377d0
NDC66993-212
Product TypeHuman Prescription Drug
Proprietary NameNilutamide
Generic NameNilutamide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2019-11-22
Marketing CategoryNDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
Application NumberNDA020169
Labeler NamePrasco Laboratories
Substance NameNILUTAMIDE
Active Ingredient Strength150 mg/1
Pharm ClassesAndrogen Receptor Antagonists [MoA],Androgen Receptor Inhibitor [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 66993-212-38

3 BLISTER PACK in 1 CARTON (66993-212-38) > 10 TABLET in 1 BLISTER PACK
Marketing Start Date2019-11-22
NDC Exclude FlagN
Sample Package?N

Drug Details

Active Ingredients

IngredientStrength
NILUTAMIDE150 mg/1

Pharmacological Class

  • Androgen Receptor Antagonists [MoA]
  • Androgen Receptor Inhibitor [EPC]

NDC Crossover Matching brand name "Nilutamide" or generic name "Nilutamide"

NDCBrand NameGeneric Name
59212-111NilandronNilutamide
62559-173NilutamideNilutamide
66993-212NilutamideNilutamide

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