Product NDC: | 0603-7608 |
Proprietary Name: | GILDESS FE 1.5/30 |
Non Proprietary Name: | norethindrone acetate, ethinyl estradiol and ferrous fumarate |
Active Ingredient(s): | & nbsp; norethindrone acetate, ethinyl estradiol and ferrous fumarate |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0603-7608 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077075 |
Marketing Category: | ANDA |
Start Marketing Date: | 20050428 |
Package NDC: | 0603-7608-17 |
Package Description: | 6 BLISTER PACK in 1 CARTON (0603-7608-17) > 1 KIT in 1 BLISTER PACK (0603-7608-01) |
NDC Code | 0603-7608-17 |
Proprietary Name | GILDESS FE 1.5/30 |
Package Description | 6 BLISTER PACK in 1 CARTON (0603-7608-17) > 1 KIT in 1 BLISTER PACK (0603-7608-01) |
Product NDC | 0603-7608 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | norethindrone acetate, ethinyl estradiol and ferrous fumarate |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20050428 |
Marketing Category Name | ANDA |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |