Flutamide - 49884-753-05 - (Flutamide)

Alphabetical Index


Drug Information of Flutamide

Product NDC: 49884-753
Proprietary Name: Flutamide
Non Proprietary Name: Flutamide
Active Ingredient(s): 125    mg/1 & nbsp;   Flutamide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Flutamide

Product NDC: 49884-753
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075298
Marketing Category: ANDA
Start Marketing Date: 20010918

Package Information of Flutamide

Package NDC: 49884-753-05
Package Description: 500 CAPSULE in 1 BOTTLE (49884-753-05)

NDC Information of Flutamide

NDC Code 49884-753-05
Proprietary Name Flutamide
Package Description 500 CAPSULE in 1 BOTTLE (49884-753-05)
Product NDC 49884-753
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Flutamide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20010918
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc.
Substance Name FLUTAMIDE
Strength Number 125
Strength Unit mg/1
Pharmaceutical Classes Androgen Receptor Antagonists [MoA],Androgen Receptor Inhibitor [EPC]

Complete Information of Flutamide


General Information