Product NDC: | 0430-0530 |
Proprietary Name: | Loestrin 24 Fe |
Non Proprietary Name: | norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
Active Ingredient(s): | & nbsp; norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0430-0530 |
Labeler Name: | Warner Chilcott (US), LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021871 |
Marketing Category: | NDA |
Start Marketing Date: | 20060301 |
Package NDC: | 0430-0530-60 |
Package Description: | 8 CARTON in 1 CASE (0430-0530-60) > 30 POUCH in 1 CARTON > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
NDC Code | 0430-0530-60 |
Proprietary Name | Loestrin 24 Fe |
Package Description | 8 CARTON in 1 CASE (0430-0530-60) > 30 POUCH in 1 CARTON > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
Product NDC | 0430-0530 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20060301 |
Marketing Category Name | NDA |
Labeler Name | Warner Chilcott (US), LLC |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |