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Junel Fe 1/20 - 54868-5326-0 - (norethindrone acetate and ethinyl estradiol, and ferrous fumarate)

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Drug Information of Junel Fe 1/20

Product NDC: 54868-5326
Proprietary Name: Junel Fe 1/20
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 Junel Fe 1/20

Product NDC: 54868-5326
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076081
Marketing Category: ANDA
Start Marketing Date: 20050603

Package Information of Junel Fe 1/20

Package NDC: 54868-5326-0
Package Description: 1 BLISTER PACK in 1 CARTON (54868-5326-0) > 1 KIT in 1 BLISTER PACK

NDC Information of Junel Fe 1/20

NDC Code 54868-5326-0
Proprietary Name Junel Fe 1/20
Package Description 1 BLISTER PACK in 1 CARTON (54868-5326-0) > 1 KIT in 1 BLISTER PACK
Product NDC 54868-5326
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 20050603
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Junel Fe 1/20


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