Product NDC: | 99207-190 |
Proprietary Name: | Estrasorb |
Non Proprietary Name: | ESTRADIOL HEMIHYDRATE |
Active Ingredient(s): | 2.5 mg/g & nbsp; ESTRADIOL HEMIHYDRATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | EMULSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 99207-190 |
Labeler Name: | Medicis Pharmaceutical Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021371 |
Marketing Category: | NDA |
Start Marketing Date: | 20120222 |
Package NDC: | 99207-190-56 |
Package Description: | 56 POUCH in 1 CARTON (99207-190-56) > 1.74 g in 1 POUCH |
NDC Code | 99207-190-56 |
Proprietary Name | Estrasorb |
Package Description | 56 POUCH in 1 CARTON (99207-190-56) > 1.74 g in 1 POUCH |
Product NDC | 99207-190 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ESTRADIOL HEMIHYDRATE |
Dosage Form Name | EMULSION |
Route Name | TOPICAL |
Start Marketing Date | 20120222 |
Marketing Category Name | NDA |
Labeler Name | Medicis Pharmaceutical Corp |
Substance Name | ESTRADIOL HEMIHYDRATE |
Strength Number | 2.5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |