Product NDC: | 47781-208 |
Proprietary Name: | Estradiol Transdermal System |
Non Proprietary Name: | Estradiol |
Active Ingredient(s): | .075 mg/d & nbsp; Estradiol |
Administration Route(s): | TRANSDERMAL |
Dosage Form(s): | PATCH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 47781-208 |
Labeler Name: | Alvogen, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020375 |
Marketing Category: | NDA |
Start Marketing Date: | 20111220 |
Package NDC: | 47781-208-04 |
Package Description: | 4 PATCH in 1 CARTON (47781-208-04) > 7 d in 1 PATCH |
NDC Code | 47781-208-04 |
Proprietary Name | Estradiol Transdermal System |
Package Description | 4 PATCH in 1 CARTON (47781-208-04) > 7 d in 1 PATCH |
Product NDC | 47781-208 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Estradiol |
Dosage Form Name | PATCH |
Route Name | TRANSDERMAL |
Start Marketing Date | 20111220 |
Marketing Category Name | NDA |
Labeler Name | Alvogen, Inc. |
Substance Name | ESTRADIOL |
Strength Number | .075 |
Strength Unit | mg/d |
Pharmaceutical Classes | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |