
USFDA APPLICATION NUMBER - 21065 / DOSAGE - TABLET;ORAL - 0.005MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| ETHINYL ESTRADIOL(UNII: 423D2T571U) (ETHINYL ESTRADIOL - UNII:423D2T571U) | ETHINYL ESTRADIOL | 2.5ug |
| NORETHINDRONE ACETATE(UNII: 9S44LIC7OJ) (NORETHINDRONE - UNII:T18F433X4S) | NORETHINDRONE ACETATE | 0.5mg |
Inactive Ingredients
| Ingredient Name | Actavis Pharma, Inc. | Allergan, Inc. |
|---|---|---|
| CALCIUM STEARATE(776XM7047L) | ||
| CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | ||
| LACTOSE MONOHYDRATE(EWQ57Q8I5X) | ||
| STARCH, CORN(O8232NY3SJ) |