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Bicalutamide - 0781-5409-10 - (Bicalutamide)

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Drug Information of Bicalutamide

Product NDC: 0781-5409
Proprietary Name: Bicalutamide
Non Proprietary Name: Bicalutamide
Active Ingredient(s): 50    mg/1 & nbsp;   Bicalutamide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Bicalutamide

Product NDC: 0781-5409
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078575
Marketing Category: ANDA
Start Marketing Date: 20090706

Package Information of Bicalutamide

Package NDC: 0781-5409-10
Package Description: 1000 TABLET in 1 BOTTLE (0781-5409-10)

NDC Information of Bicalutamide

NDC Code 0781-5409-10
Proprietary Name Bicalutamide
Package Description 1000 TABLET in 1 BOTTLE (0781-5409-10)
Product NDC 0781-5409
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bicalutamide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090706
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name BICALUTAMIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Androgen Receptor Antagonists [MoA],Androgen Receptor Inhibitor [EPC]

Complete Information of Bicalutamide


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