Home
>
National Drug Code (NDC)
>
Kurvelo
Kurvelo - 68180-844-13 - (Levonorgestrel and Ethinyl Estradiol)
Drug Information of Kurvelo
| Product NDC: | 68180-844 |
| Proprietary Name: | Kurvelo |
| 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) |
Labeler Information of Kurvelo
| Product NDC: | 68180-844 |
| Labeler Name: | Lupin Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091440 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121025 |
Package Information of Kurvelo
| Package NDC: | 68180-844-13 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68180-844-13) > 1 KIT in 1 BLISTER PACK (68180-844-11) |
NDC Information of Kurvelo
| NDC Code | 68180-844-13 |
| Proprietary Name | Kurvelo |
| Package Description | 3 BLISTER PACK in 1 CARTON (68180-844-13) > 1 KIT in 1 BLISTER PACK (68180-844-11) |
| Product NDC | 68180-844 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levonorgestrel and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20121025 |
| Marketing Category Name | ANDA |
| Labeler Name | Lupin Pharmaceuticals, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
