ESTRACE - 0430-0721-24 - (estradiol)

Alphabetical Index


Drug Information of ESTRACE

Product NDC: 0430-0721
Proprietary Name: ESTRACE
Non Proprietary Name: estradiol
Active Ingredient(s): 1    mg/1 & nbsp;   estradiol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ESTRACE

Product NDC: 0430-0721
Labeler Name: Warner Chilcott (US), LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040197
Marketing Category: ANDA
Start Marketing Date: 20111226

Package Information of ESTRACE

Package NDC: 0430-0721-24
Package Description: 100 TABLET in 1 BOTTLE (0430-0721-24)

NDC Information of ESTRACE

NDC Code 0430-0721-24
Proprietary Name ESTRACE
Package Description 100 TABLET in 1 BOTTLE (0430-0721-24)
Product NDC 0430-0721
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name estradiol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111226
Marketing Category Name ANDA
Labeler Name Warner Chilcott (US), LLC
Substance Name ESTRADIOL
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA]

Complete Information of ESTRACE


General Information