NDC Code | 0603-7606-48 |
Package Description | 3 BLISTER PACK in 1 CARTON (0603-7606-48) > 21 TABLET, FILM COATED in 1 BLISTER PACK (0603-7606-02) |
Product NDC | 0603-7606 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Gildess 1.5/30 |
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 | ANDA077075 |
Manufacturer | Par Pharmaceutical |
Substance Name | NORETHINDRONE ACETATE; ETHINYL ESTRADIOL |
Strength | 1.5; .03 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |