FEMCON Fe - 54868-6161-0 - (norethindrone and ethinyl estradiol, and ferrous fumarate)

Alphabetical Index


Drug Information of FEMCON Fe

Product NDC: 54868-6161
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: 54868-6161
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021490
Marketing Category: NDA
Start Marketing Date: 20100921

Package Information of FEMCON Fe

Package NDC: 54868-6161-0
Package Description: 1 BLISTER PACK in 1 CELLO PACK (54868-6161-0) > 1 KIT in 1 BLISTER PACK

NDC Information of FEMCON Fe

NDC Code 54868-6161-0
Proprietary Name FEMCON Fe
Package Description 1 BLISTER PACK in 1 CELLO PACK (54868-6161-0) > 1 KIT in 1 BLISTER PACK
Product NDC 54868-6161
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 20100921
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of FEMCON Fe


General Information