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 ID: 66993-212_827f3aa0-e545-4678-be80-1a2d492377d0
• NDC: 66993-212
• Product Type: Human Prescription Drug
• Proprietary Name: Nilutamide
• Generic Name: Nilutamide
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2019-11-22
• Marketing Category: NDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
• Application Number: NDA020169
• Labeler Name: Prasco Laboratories
• Substance Name: NILUTAMIDE
• Active Ingredient Strength: 150 mg/1
• Pharm Classes: Androgen Receptor Antagonists [MoA],Androgen Receptor Inhibitor [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 66993-212-38

3 BLISTER PACK in 1 CARTON (66993-212-38) > 10 TABLET in 1 BLISTER PACK

• Marketing Start Date: 2019-11-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 66993-212-38 [66993021238]

Nilutamide TABLET

• Marketing Category: NDA AUTHORIZED GENERIC
• Application Number: NDA020169
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2019-11-22

Drug Details

Active Ingredients

Ingredient	Strength
NILUTAMIDE	150 mg/1

Pharmacological Class

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

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

NDC	Brand Name	Generic Name
62559-173	Nilutamide	Nilutamide
66993-212	Nilutamide	Nilutamide
82454-0212	Nilutamide	Nilutamide
59212-111	Nilandron	Nilutamide
82454-0111	Nilandron	Nilutamide