Estradiol - 54868-4030-2 - (Estradiol)

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Drug Information of Estradiol

Product NDC: 54868-4030
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: 54868-4030
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040197
Marketing Category: ANDA
Start Marketing Date: 20000918

Package Information of Estradiol

Package NDC: 54868-4030-2
Package Description: 90 TABLET in 1 BOTTLE (54868-4030-2)

NDC Information of Estradiol

NDC Code 54868-4030-2
Proprietary Name Estradiol
Package Description 90 TABLET in 1 BOTTLE (54868-4030-2)
Product NDC 54868-4030
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Estradiol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000918
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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