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: | 0430-0570-60 |
Package Description: | 10 CARTON in 1 CASE (0430-0570-60) > 30 CELLO PACK in 1 CARTON > 1 BLISTER PACK in 1 CELLO PACK > 1 KIT in 1 BLISTER PACK |
NDC Code | 0430-0570-60 |
Proprietary Name | ESTROSTEP Fe |
Package Description | 10 CARTON in 1 CASE (0430-0570-60) > 30 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 |
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Strength Number | |
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