| Product NDC: | 0169-5176 |
| Proprietary Name: | Vagifem |
| Non Proprietary Name: | estradiol |
| Active Ingredient(s): | 10 ug/1 & nbsp; estradiol |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0169-5176 |
| Labeler Name: | Novo Nordisk |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020908 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100111 |
| Package NDC: | 0169-5176-03 |
| Package Description: | 8 APPLICATOR in 1 CARTON (0169-5176-03) > 1 TABLET, FILM COATED in 1 APPLICATOR |
| NDC Code | 0169-5176-03 |
| Proprietary Name | Vagifem |
| Package Description | 8 APPLICATOR in 1 CARTON (0169-5176-03) > 1 TABLET, FILM COATED in 1 APPLICATOR |
| Product NDC | 0169-5176 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | estradiol |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | VAGINAL |
| Start Marketing Date | 20100111 |
| Marketing Category Name | NDA |
| Labeler Name | Novo Nordisk |
| Substance Name | ESTRADIOL |
| Strength Number | 10 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |