| Product NDC: | 51285-058 |
| Proprietary Name: | Seasonale |
| Non Proprietary Name: | levonorgestrel / ethinyl estradiol |
| Active Ingredient(s): | & nbsp; levonorgestrel / ethinyl estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51285-058 |
| Labeler Name: | Duramed Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021544 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030509 |
| Package NDC: | 51285-058-66 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (51285-058-66) > 1 KIT in 1 BLISTER PACK |
| NDC Code | 51285-058-66 |
| Proprietary Name | Seasonale |
| Package Description | 3 BLISTER PACK in 1 CARTON (51285-058-66) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 51285-058 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levonorgestrel / ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20030509 |
| Marketing Category Name | NDA |
| Labeler Name | Duramed Pharmaceuticals, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |