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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