Evista - 54868-4170-1 - (Raloxifene hydrochloride)

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Drug Information of Evista

Product NDC: 54868-4170
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: 54868-4170
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020815
Marketing Category: NDA
Start Marketing Date: 20000511

Package Information of Evista

Package NDC: 54868-4170-1
Package Description: 60 TABLET in 1 BOTTLE (54868-4170-1)

NDC Information of Evista

NDC Code 54868-4170-1
Proprietary Name Evista
Package Description 60 TABLET in 1 BOTTLE (54868-4170-1)
Product NDC 54868-4170
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Raloxifene hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000511
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
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