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ESTROSTEP Fe - 0430-0570-45 - (Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate)

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Drug Information of ESTROSTEP Fe

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)

Labeler Information of ESTROSTEP Fe

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 Information of ESTROSTEP Fe

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 Information of ESTROSTEP Fe

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
Pharmaceutical Classes

Complete Information of ESTROSTEP Fe


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