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Loestrin 24 Fe
Loestrin 24 Fe - 0430-0530-95 - (norethindrone acetate and ethinyl estradiol, and ferrous fumarate)
Drug Information of Loestrin 24 Fe
| 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) |
Labeler Information of Loestrin 24 Fe
| 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 Information of Loestrin 24 Fe
| Package NDC: | 0430-0530-95 |
| Package Description: | 30 TRAY in 1 CASE (0430-0530-95) > 6 CARTON in 1 TRAY > 1 POUCH in 1 CARTON > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
NDC Information of Loestrin 24 Fe
| NDC Code | 0430-0530-95 |
| Proprietary Name | Loestrin 24 Fe |
| Package Description | 30 TRAY in 1 CASE (0430-0530-95) > 6 CARTON in 1 TRAY > 1 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 |
