FEMCON Fe - 0430-0482-14 - (norethindrone and ethinyl estradiol, and ferrous fumarate)

Alphabetical Index


Drug Information of FEMCON Fe

Product NDC: 0430-0482
Proprietary Name: FEMCON Fe
Non Proprietary Name: norethindrone and ethinyl estradiol, and ferrous fumarate
Active Ingredient(s):    & nbsp;   norethindrone and ethinyl estradiol, and ferrous fumarate
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of FEMCON Fe

Product NDC: 0430-0482
Labeler Name: Warner Chilcott (US), LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021490
Marketing Category: NDA
Start Marketing Date: 20061101

Package Information of FEMCON Fe

Package NDC: 0430-0482-14
Package Description: 72 CARTON in 1 CASE (0430-0482-14) > 5 CELLO PACK in 1 CARTON > 1 BLISTER PACK in 1 CELLO PACK > 1 KIT in 1 BLISTER PACK

NDC Information of FEMCON Fe

NDC Code 0430-0482-14
Proprietary Name FEMCON Fe
Package Description 72 CARTON in 1 CASE (0430-0482-14) > 5 CELLO PACK in 1 CARTON > 1 BLISTER PACK in 1 CELLO PACK > 1 KIT in 1 BLISTER PACK
Product NDC 0430-0482
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name norethindrone and ethinyl estradiol, and ferrous fumarate
Dosage Form Name KIT
Route Name
Start Marketing Date 20061101
Marketing Category Name NDA
Labeler Name Warner Chilcott (US), LLC
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of FEMCON Fe


General Information