Estradiol - 55289-603-21 - (estradiol)

Alphabetical Index


Drug Information of Estradiol

Product NDC: 55289-603
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: 55289-603
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040326
Marketing Category: ANDA
Start Marketing Date: 20091217

Package Information of Estradiol

Package NDC: 55289-603-21
Package Description: 21 TABLET in 1 BOTTLE, PLASTIC (55289-603-21)

NDC Information of Estradiol

NDC Code 55289-603-21
Proprietary Name Estradiol
Package Description 21 TABLET in 1 BOTTLE, PLASTIC (55289-603-21)
Product NDC 55289-603
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name estradiol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091217
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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