Home
>
National Drug Code (NDC)
>
Menostar
Menostar - 50419-455-04 - (estradiol)
Drug Information of Menostar
| Product NDC: | 50419-455 |
| Proprietary Name: | Menostar |
| Non Proprietary Name: | estradiol |
| Active Ingredient(s): | 14 ug/1 & nbsp; estradiol |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Menostar
| Product NDC: | 50419-455 |
| Labeler Name: | Bayer HealthCare Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020375 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040608 |
Package Information of Menostar
| Package NDC: | 50419-455-04 |
| Package Description: | 4 PATCH in 1 CARTON (50419-455-04) |
NDC Information of Menostar
| NDC Code | 50419-455-04 |
| Proprietary Name | Menostar |
| Package Description | 4 PATCH in 1 CARTON (50419-455-04) |
| Product NDC | 50419-455 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | estradiol |
| Dosage Form Name | PATCH |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20040608 |
| Marketing Category Name | NDA |
| Labeler Name | Bayer HealthCare Pharmaceuticals Inc. |
| Substance Name | ESTRADIOL |
| Strength Number | 14 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
