Estradiol - 23155-014-05 - (Estradiol)

Alphabetical Index


Drug Information of Estradiol

Product NDC: 23155-014
Proprietary Name: Estradiol
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 Estradiol

Product NDC: 23155-014
Labeler Name: Heritage Pharmaceuticals Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040275
Marketing Category: ANDA
Start Marketing Date: 20101105

Package Information of Estradiol

Package NDC: 23155-014-05
Package Description: 500 TABLET in 1 BOTTLE (23155-014-05)

NDC Information of Estradiol

NDC Code 23155-014-05
Proprietary Name Estradiol
Package Description 500 TABLET in 1 BOTTLE (23155-014-05)
Product NDC 23155-014
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Estradiol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101105
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc
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 Estradiol


General Information