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Zenchent FE - 52544-292-31 - (Norethindrone and Ethinyl Estradiol)

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Drug Information of Zenchent FE

Product NDC: 52544-292
Proprietary Name: Zenchent FE
Non Proprietary Name: Norethindrone and Ethinyl Estradiol
Active Ingredient(s):    & nbsp;   Norethindrone and Ethinyl Estradiol
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Zenchent FE

Product NDC: 52544-292
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078892
Marketing Category: ANDA
Start Marketing Date: 20110926

Package Information of Zenchent FE

Package NDC: 52544-292-31
Package Description: 3 BLISTER PACK in 1 CARTON (52544-292-31) > 1 KIT in 1 BLISTER PACK (52544-292-41)

NDC Information of Zenchent FE

NDC Code 52544-292-31
Proprietary Name Zenchent FE
Package Description 3 BLISTER PACK in 1 CARTON (52544-292-31) > 1 KIT in 1 BLISTER PACK (52544-292-41)
Product NDC 52544-292
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norethindrone and Ethinyl Estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20110926
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Zenchent FE


General Information