ESTRACE - 54868-0496-0 - (estradiol)

Alphabetical Index


Drug Information of ESTRACE

Product NDC: 54868-0496
Proprietary Name: ESTRACE
Non Proprietary Name: estradiol
Active Ingredient(s): .1    mg/g & nbsp;   estradiol
Administration Route(s): VAGINAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of ESTRACE

Product NDC: 54868-0496
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086069
Marketing Category: ANDA
Start Marketing Date: 20030614

Package Information of ESTRACE

Package NDC: 54868-0496-0
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON (54868-0496-0) > 42.5 g in 1 TUBE, WITH APPLICATOR

NDC Information of ESTRACE

NDC Code 54868-0496-0
Proprietary Name ESTRACE
Package Description 1 TUBE, WITH APPLICATOR in 1 CARTON (54868-0496-0) > 42.5 g in 1 TUBE, WITH APPLICATOR
Product NDC 54868-0496
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name estradiol
Dosage Form Name CREAM
Route Name VAGINAL
Start Marketing Date 20030614
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ESTRADIOL
Strength Number .1
Strength Unit mg/g
Pharmaceutical Classes Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA]

Complete Information of ESTRACE


General Information