Product NDC: | 54868-6182 |
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: | 54868-6182 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020908 |
Marketing Category: | NDA |
Start Marketing Date: | 20100924 |
Package NDC: | 54868-6182-0 |
Package Description: | 8 APPLICATOR in 1 CARTON (54868-6182-0) > 1 TABLET, FILM COATED in 1 APPLICATOR |
NDC Code | 54868-6182-0 |
Proprietary Name | Vagifem |
Package Description | 8 APPLICATOR in 1 CARTON (54868-6182-0) > 1 TABLET, FILM COATED in 1 APPLICATOR |
Product NDC | 54868-6182 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | estradiol |
Dosage Form Name | TABLET, FILM COATED |
Route Name | VAGINAL |
Start Marketing Date | 20100924 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | ESTRADIOL |
Strength Number | 10 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |