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Loestrin 24 Fe - 54868-6100-0 - (norethindrone acetate and ethinyl estradiol, and ferrous fumarate)

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Drug Information of Loestrin 24 Fe

Product NDC: 54868-6100
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: 54868-6100
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021871
Marketing Category: NDA
Start Marketing Date: 20100128

Package Information of Loestrin 24 Fe

Package NDC: 54868-6100-0
Package Description: 1 BLISTER PACK in 1 POUCH (54868-6100-0) > 1 KIT in 1 BLISTER PACK

NDC Information of Loestrin 24 Fe

NDC Code 54868-6100-0
Proprietary Name Loestrin 24 Fe
Package Description 1 BLISTER PACK in 1 POUCH (54868-6100-0) > 1 KIT in 1 BLISTER PACK
Product NDC 54868-6100
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 20100128
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Loestrin 24 Fe


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