Estradiol - 21695-613-00 - (Estradiol)

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Drug Information of Estradiol

Product NDC: 21695-613
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: 21695-613
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040114
Marketing Category: ANDA
Start Marketing Date: 19960314

Package Information of Estradiol

Package NDC: 21695-613-00
Package Description: 100 TABLET in 1 BOTTLE (21695-613-00)

NDC Information of Estradiol

NDC Code 21695-613-00
Proprietary Name Estradiol
Package Description 100 TABLET in 1 BOTTLE (21695-613-00)
Product NDC 21695-613
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 Rebel Distributors Corp
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