AVODART - 0173-0712-15 - (dutasteride)

Alphabetical Index


Drug Information of AVODART

Product NDC: 0173-0712
Proprietary Name: AVODART
Non Proprietary Name: dutasteride
Active Ingredient(s): .5    mg/1 & nbsp;   dutasteride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of AVODART

Product NDC: 0173-0712
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021319
Marketing Category: NDA
Start Marketing Date: 20021210

Package Information of AVODART

Package NDC: 0173-0712-15
Package Description: 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (0173-0712-15)

NDC Information of AVODART

NDC Code 0173-0712-15
Proprietary Name AVODART
Package Description 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (0173-0712-15)
Product NDC 0173-0712
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dutasteride
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20021210
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name DUTASTERIDE
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

Complete Information of AVODART


General Information