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Levonorgestrel and Ethinyl Estradiol
Levonorgestrel and Ethinyl Estradiol - 68180-854-13 - (Levonorgestrel and Ethinyl Estradiol)
Drug Information of Levonorgestrel and Ethinyl Estradiol
| Product NDC: | 68180-854 |
| Proprietary Name: | Levonorgestrel 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) |
Labeler Information of Levonorgestrel and Ethinyl Estradiol
| Product NDC: | 68180-854 |
| Labeler Name: | Lupin Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091425 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130320 |
Package Information of Levonorgestrel and Ethinyl Estradiol
| Package NDC: | 68180-854-13 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68180-854-13) > 1 KIT in 1 BLISTER PACK (68180-854-11) |
NDC Information of Levonorgestrel and Ethinyl Estradiol
| NDC Code | 68180-854-13 |
| Proprietary Name | Levonorgestrel and Ethinyl Estradiol |
| Package Description | 3 BLISTER PACK in 1 CARTON (68180-854-13) > 1 KIT in 1 BLISTER PACK (68180-854-11) |
| Product NDC | 68180-854 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levonorgestrel and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20130320 |
| Marketing Category Name | ANDA |
| Labeler Name | Lupin Pharmaceuticals, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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