Alora - 52544-471-08 - (Estradiol Transdermal System)

Alphabetical Index


Drug Information of Alora

Product NDC: 52544-471
Proprietary Name: Alora
Non Proprietary Name: Estradiol Transdermal System
Active Ingredient(s): .05    mg/d & nbsp;   Estradiol Transdermal System
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of Alora

Product NDC: 52544-471
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020655
Marketing Category: NDA
Start Marketing Date: 19961220

Package Information of Alora

Package NDC: 52544-471-08
Package Description: 8 POUCH in 1 BOX (52544-471-08) > 1 PATCH in 1 POUCH > 3.5 d in 1 PATCH

NDC Information of Alora

NDC Code 52544-471-08
Proprietary Name Alora
Package Description 8 POUCH in 1 BOX (52544-471-08) > 1 PATCH in 1 POUCH > 3.5 d in 1 PATCH
Product NDC 52544-471
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Estradiol Transdermal System
Dosage Form Name PATCH
Route Name TRANSDERMAL
Start Marketing Date 19961220
Marketing Category Name NDA
Labeler Name Watson Pharma, Inc.
Substance Name ESTRADIOL
Strength Number .05
Strength Unit mg/d
Pharmaceutical Classes Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA]

Complete Information of Alora


General Information