| Product NDC: | 0430-0570 |
| Proprietary Name: | ESTROSTEP 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: | 0430-0570 |
| Labeler Name: | Warner Chilcott (US), LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020130 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050419 |
| Package NDC: | 0430-0570-45 |
| Package Description: | 72 CARTON in 1 CASE (0430-0570-45) > 3 CELLO PACK in 1 CARTON > 1 BLISTER PACK in 1 CELLO PACK > 1 KIT in 1 BLISTER PACK |
| NDC Code | 0430-0570-45 |
| Proprietary Name | ESTROSTEP Fe |
| Package Description | 72 CARTON in 1 CASE (0430-0570-45) > 3 CELLO PACK in 1 CARTON > 1 BLISTER PACK in 1 CELLO PACK > 1 KIT in 1 BLISTER PACK |
| Product NDC | 0430-0570 |
| 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 | 20050419 |
| Marketing Category Name | NDA |
| Labeler Name | Warner Chilcott (US), LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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