| Product NDC: | 50419-405 |
| Proprietary Name: | Yaz |
| Non Proprietary Name: | Drospirenone and ethinyl estradiol |
| Active Ingredient(s): | & nbsp; Drospirenone and ethinyl estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50419-405 |
| Labeler Name: | Bayer HealthCare Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021676 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060316 |
| Package NDC: | 50419-405-03 |
| Package Description: | 3 BLISTER PACK in 1 PACKAGE (50419-405-03) > 1 KIT in 1 BLISTER PACK |
| NDC Code | 50419-405-03 |
| Proprietary Name | Yaz |
| Package Description | 3 BLISTER PACK in 1 PACKAGE (50419-405-03) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 50419-405 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Drospirenone and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20060316 |
| Marketing Category Name | NDA |
| Labeler Name | Bayer HealthCare Pharmaceuticals Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |