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Lessina
Lessina - 0555-9013-57 - (levonorgestrel and ethinyl estradiol)
Drug Information of Lessina
| Product NDC: | 0555-9013 |
| Proprietary Name: | Lessina |
| Non Proprietary Name: | levonorgestrel and ethinyl estradiol |
| Active Ingredient(s): | .02; .1 mg/1; mg/1 & nbsp; levonorgestrel and ethinyl estradiol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lessina
| Product NDC: | 0555-9013 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075803 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020422 |
Package Information of Lessina
| Package NDC: | 0555-9013-57 |
| Package Description: | 6 POUCH in 1 CARTON (0555-9013-57) > 1 BLISTER PACK in 1 POUCH > 21 TABLET in 1 BLISTER PACK |
NDC Information of Lessina
| NDC Code | 0555-9013-57 |
| Proprietary Name | Lessina |
| Package Description | 6 POUCH in 1 CARTON (0555-9013-57) > 1 BLISTER PACK in 1 POUCH > 21 TABLET in 1 BLISTER PACK |
| Product NDC | 0555-9013 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levonorgestrel and ethinyl estradiol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20020422 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | ETHINYL ESTRADIOL; LEVONORGESTREL |
| Strength Number | .02; .1 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Inhibit Ovum Fertilization [PE],Progesterone Congeners [Chemical/Ingredient],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Progestin-containing Intrauterine Device [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
