Estradiol - 63629-2766-1 - (Estradiol)

Alphabetical Index


Drug Information of Estradiol

Product NDC: 63629-2766
Proprietary Name: Estradiol
Non Proprietary Name: Estradiol
Active Ingredient(s): .5    mg/1 & nbsp;   Estradiol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Estradiol

Product NDC: 63629-2766
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040114
Marketing Category: ANDA
Start Marketing Date: 19960314

Package Information of Estradiol

Package NDC: 63629-2766-1
Package Description: 1 TABLET in 1 BOTTLE (63629-2766-1)

NDC Information of Estradiol

NDC Code 63629-2766-1
Proprietary Name Estradiol
Package Description 1 TABLET in 1 BOTTLE (63629-2766-1)
Product NDC 63629-2766
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Estradiol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960314
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name ESTRADIOL
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA]

Complete Information of Estradiol


General Information