| Product NDC: | 51285-092 |
| Proprietary Name: | LoSeasonique |
| Non Proprietary Name: | levonorgestrel/ethinyl estradiol and ethinyl estradiol |
| Active Ingredient(s): | & nbsp; levonorgestrel/ethinyl estradiol and ethinyl estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51285-092 |
| Labeler Name: | Teva Women's Health, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022262 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20081024 |
| Package NDC: | 51285-092-87 |
| Package Description: | 2 BLISTER PACK in 1 BOX (51285-092-87) > 1 KIT in 1 BLISTER PACK |
| NDC Code | 51285-092-87 |
| Proprietary Name | LoSeasonique |
| Package Description | 2 BLISTER PACK in 1 BOX (51285-092-87) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 51285-092 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levonorgestrel/ethinyl estradiol and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20081024 |
| Marketing Category Name | NDA |
| Labeler Name | Teva Women's Health, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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