| NDC Code | 0603-7607-15 |
|---|
| Package Description | 6 BLISTER PACK in 1 CARTON (0603-7607-15) > 21 TABLET, FILM COATED in 1 BLISTER PACK (0603-7607-02) |
|---|
| Product NDC | 0603-7607 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Gildess 1/20 |
|---|
| Non-Proprietary Name | Norethindrone Acetate And Ethinyl Estradiol |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20120724 |
|---|
| End Marketing Date | 20180331 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077077 |
|---|
| Manufacturer | Par Pharmaceutical |
|---|
| Substance Name | NORETHINDRONE ACETATE; ETHINYL ESTRADIOL |
|---|
| Strength | 1; .02 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
|---|