| Product NDC: | 68180-848 |
| Proprietary Name: | Levonorgestrel and Ethinyl Estradiol and Ethinyl Estradiol |
| Non Proprietary Name: | levonorgestrel and ethinyl estradiol |
| Active Ingredient(s): | & nbsp; levonorgestrel and ethinyl estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68180-848 |
| Labeler Name: | LUPIN PHARMACEUTICALS INC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091674 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111202 |
| Package NDC: | 68180-848-13 |
| Package Description: | 2 POUCH in 1 CARTON (68180-848-13) > 1 BLISTER PACK in 1 POUCH (68180-848-11) > 1 KIT in 1 BLISTER PACK |
| NDC Code | 68180-848-13 |
| Proprietary Name | Levonorgestrel and Ethinyl Estradiol and Ethinyl Estradiol |
| Package Description | 2 POUCH in 1 CARTON (68180-848-13) > 1 BLISTER PACK in 1 POUCH (68180-848-11) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 68180-848 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levonorgestrel and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20111202 |
| Marketing Category Name | ANDA |
| Labeler Name | LUPIN PHARMACEUTICALS INC |
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