| 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: | 99207-190-01 |
| Package Description: | 14 POUCH in 1 CARTON (99207-190-01) > 1.74 g in 1 POUCH |
| NDC Code | 99207-190-01 |
| Proprietary Name | Estrasorb |
| Package Description | 14 POUCH in 1 CARTON (99207-190-01) > 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] |