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GILDESS FE 1/20
GILDESS FE 1/20 - 0603-7609-17 - (norethindrone acetate, ethinyl estradiol and ferrous fumarate)
Drug Information of GILDESS FE 1/20
| Product NDC: | 0603-7609 |
| Proprietary Name: | GILDESS FE 1/20 |
| 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) |
Labeler Information of GILDESS FE 1/20
| Product NDC: | 0603-7609 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077077 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050520 |
Package Information of GILDESS FE 1/20
| Package NDC: | 0603-7609-17 |
| Package Description: | 6 BLISTER PACK in 1 CARTON (0603-7609-17) > 1 KIT in 1 BLISTER PACK (0603-7609-01) |
NDC Information of GILDESS FE 1/20
| NDC Code | 0603-7609-17 |
| Proprietary Name | GILDESS FE 1/20 |
| Package Description | 6 BLISTER PACK in 1 CARTON (0603-7609-17) > 1 KIT in 1 BLISTER PACK (0603-7609-01) |
| Product NDC | 0603-7609 |
| 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 | 20050520 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
