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Yasmin
Yasmin - 50419-402-03 - (drospirenone and ethinyl estradiol)
Drug Information of Yasmin
| Product NDC: | 50419-402 |
| Proprietary Name: | Yasmin |
| 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) |
Labeler Information of Yasmin
| Product NDC: | 50419-402 |
| Labeler Name: | Bayer HealthCare Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021098 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20010511 |
Package Information of Yasmin
| Package NDC: | 50419-402-03 |
| Package Description: | 3 BLISTER PACK in 1 PACKAGE (50419-402-03) > 1 KIT in 1 BLISTER PACK |
NDC Information of Yasmin
| NDC Code | 50419-402-03 |
| Proprietary Name | Yasmin |
| Package Description | 3 BLISTER PACK in 1 PACKAGE (50419-402-03) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 50419-402 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | drospirenone and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20010511 |
| Marketing Category Name | NDA |
| Labeler Name | Bayer HealthCare Pharmaceuticals Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
