Evista - 0002-4165-07 - (Raloxifene hydrochloride)

Alphabetical Index


Drug Information of Evista

Product NDC: 0002-4165
Proprietary Name: Evista
Non Proprietary Name: Raloxifene hydrochloride
Active Ingredient(s): 60    mg/1 & nbsp;   Raloxifene hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Evista

Product NDC: 0002-4165
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020815
Marketing Category: NDA
Start Marketing Date: 19980106

Package Information of Evista

Package NDC: 0002-4165-07
Package Description: 2000 TABLET in 1 BOTTLE (0002-4165-07)

NDC Information of Evista

NDC Code 0002-4165-07
Proprietary Name Evista
Package Description 2000 TABLET in 1 BOTTLE (0002-4165-07)
Product NDC 0002-4165
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Raloxifene hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19980106
Marketing Category Name NDA
Labeler Name Eli Lilly and Company
Substance Name RALOXIFENE HYDROCHLORIDE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA]

Complete Information of Evista


General Information