Product NDC: | 18860-490 |
Proprietary Name: | Elestrin |
Non Proprietary Name: | estradiol |
Active Ingredient(s): | .6 mg/g & nbsp; estradiol |
Administration Route(s): | TRANSDERMAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 18860-490 |
Labeler Name: | Jazz Pharmaceuticals Commercial Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021813 |
Marketing Category: | NDA |
Start Marketing Date: | 20070601 |
Package NDC: | 18860-490-02 |
Package Description: | 1 BOTTLE, PUMP in 1 CARTON (18860-490-02) > 144 g in 1 BOTTLE, PUMP |
NDC Code | 18860-490-02 |
Proprietary Name | Elestrin |
Package Description | 1 BOTTLE, PUMP in 1 CARTON (18860-490-02) > 144 g in 1 BOTTLE, PUMP |
Product NDC | 18860-490 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | estradiol |
Dosage Form Name | GEL |
Route Name | TRANSDERMAL |
Start Marketing Date | 20070601 |
Marketing Category Name | NDA |
Labeler Name | Jazz Pharmaceuticals Commercial Corp. |
Substance Name | ESTRADIOL |
Strength Number | .6 |
Strength Unit | mg/g |
Pharmaceutical Classes | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |