| NDC Code | 0555-9027-42 |
|---|
| Package Description | 3 POUCH in 1 CARTON (0555-9027-42) / 1 BLISTER PACK in 1 POUCH / 21 TABLET in 1 BLISTER PACK |
|---|
| Product NDC | 0555-9027 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Junel |
|---|
| Proprietary Name Suffix | 21 Day |
|---|
| Non-Proprietary Name | Norethindrone Acetate And Ethinyl Estradiol |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20030918 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076381 |
|---|
| Manufacturer | Teva Pharmaceuticals USA, Inc. |
|---|
| Substance Name | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE |
|---|
| Strength | 30; 1.5 |
|---|
| Strength Unit | ug/1; mg/1 |
|---|
| Pharmacy Classes | Estrogen Receptor Agonists [MoA], Estrogen [EPC], Progesterone Congeners [CS], Progestin [EPC] |
|---|