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 | |
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