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 |