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Zovia 1/35E-28 - 52544-383-28 - (Ethynodiol Diacetate and Ethinyl Estradiol)

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Drug Information of Zovia 1/35E-28

Product NDC: 52544-383
Proprietary Name: Zovia 1/35E-28
Non Proprietary Name: Ethynodiol Diacetate and Ethinyl Estradiol
Active Ingredient(s):    & nbsp;   Ethynodiol Diacetate and Ethinyl Estradiol
Administration Route(s): ORAL
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Zovia 1/35E-28

Product NDC: 52544-383
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072721
Marketing Category: ANDA
Start Marketing Date: 19911230

Package Information of Zovia 1/35E-28

Package NDC: 52544-383-28
Package Description: 6 BLISTER PACK in 1 CARTON (52544-383-28) > 1 KIT in 1 BLISTER PACK

NDC Information of Zovia 1/35E-28

NDC Code 52544-383-28
Proprietary Name Zovia 1/35E-28
Package Description 6 BLISTER PACK in 1 CARTON (52544-383-28) > 1 KIT in 1 BLISTER PACK
Product NDC 52544-383
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ethynodiol Diacetate and Ethinyl Estradiol
Dosage Form Name KIT
Route Name ORAL
Start Marketing Date 19911230
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
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Complete Information of Zovia 1/35E-28


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