CASODEX - 0310-0705-10 - (Bicalutamide)

Alphabetical Index


Drug Information of CASODEX

Product NDC: 0310-0705
Proprietary Name: CASODEX
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 CASODEX

Product NDC: 0310-0705
Labeler Name: AstraZeneca Pharmaceuticals LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020498
Marketing Category: NDA
Start Marketing Date: 19951016

Package Information of CASODEX

Package NDC: 0310-0705-10
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0310-0705-10)

NDC Information of CASODEX

NDC Code 0310-0705-10
Proprietary Name CASODEX
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0310-0705-10)
Product NDC 0310-0705
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bicalutamide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19951016
Marketing Category Name NDA
Labeler Name AstraZeneca Pharmaceuticals LP
Substance Name BICALUTAMIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Androgen Receptor Antagonists [MoA],Androgen Receptor Inhibitor [EPC]

Complete Information of CASODEX


General Information