Home > National Drug Code (NDC) > Loestrin 24 Fe

Loestrin 24 Fe - 0430-0530-95 - (norethindrone acetate and ethinyl estradiol, and ferrous fumarate)

Alphabetical Index


Drug Information of Loestrin 24 Fe

Product NDC: 0430-0530
Proprietary Name: Loestrin 24 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 Loestrin 24 Fe

Product NDC: 0430-0530
Labeler Name: Warner Chilcott (US), LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021871
Marketing Category: NDA
Start Marketing Date: 20060301

Package Information of Loestrin 24 Fe

Package NDC: 0430-0530-95
Package Description: 30 TRAY in 1 CASE (0430-0530-95) > 6 CARTON in 1 TRAY > 1 POUCH in 1 CARTON > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK

NDC Information of Loestrin 24 Fe

NDC Code 0430-0530-95
Proprietary Name Loestrin 24 Fe
Package Description 30 TRAY in 1 CASE (0430-0530-95) > 6 CARTON in 1 TRAY > 1 POUCH in 1 CARTON > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK
Product NDC 0430-0530
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 20060301
Marketing Category Name NDA
Labeler Name Warner Chilcott (US), LLC
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Loestrin 24 Fe


General Information