| NDC Code | 0555-9009-42 |
|---|
| Package Description | 3 POUCH in 1 CARTON (0555-9009-42) / 1 BLISTER PACK in 1 POUCH (0555-9009-80) / 21 TABLET in 1 BLISTER PACK |
|---|
| Product NDC | 0555-9009 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Nortrel |
|---|
| Proprietary Name Suffix | 21 Day |
|---|
| Non-Proprietary Name | Norethindrone And Ethinyl Estradiol |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20010613 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA072693 |
|---|
| Manufacturer | Teva Pharmaceuticals USA, Inc. |
|---|
| Substance Name | ETHINYL ESTRADIOL; NORETHINDRONE |
|---|
| Strength | .035; 1 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Estrogen Receptor Agonists [MoA], Estrogen [EPC], Progesterone Congeners [CS], Progestin [EPC] |
|---|