LOESTRIN 1/20 - norethindrone acetate and ethinyl estradiol
Navigation: NDC > Supplier starting with: T > TEVA WOMEN'S HEALTH, INC| Field | Value |
|---|---|
| NDC Code: | 51285-079 |
| Proprietary Name: | LOESTRIN 1/20 |
| Suffix: | 21 Day |
| Non-Proprietary Name: | norethindrone acetate and ethinyl estradiol |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 01-10-2008 |
| Category Name: | ANDA |
| Application Number: | ANDA076380 |
| Labeler: | TEVA WOMEN'S HEALTH, INC |
| Substance Name: | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE |
| Active Numerator Strength: | 20; 1 |
| Active Ingredient Unit: | ug/1; mg/1 |
| Pharm Classes: | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
| DEA Schedule: |