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Zovia 1/35E-28 - 54868-4240-0 - (Ethynodiol Diacetate and Ethinyl Estradiol)

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Drug Information of Zovia 1/35E-28

Product NDC: 54868-4240
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: 54868-4240
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072721
Marketing Category: ANDA
Start Marketing Date: 20030623

Package Information of Zovia 1/35E-28

Package NDC: 54868-4240-0
Package Description: 1 BLISTER PACK in 1 CONTAINER (54868-4240-0) > 1 KIT in 1 BLISTER PACK

NDC Information of Zovia 1/35E-28

NDC Code 54868-4240-0
Proprietary Name Zovia 1/35E-28
Package Description 1 BLISTER PACK in 1 CONTAINER (54868-4240-0) > 1 KIT in 1 BLISTER PACK
Product NDC 54868-4240
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ethynodiol Diacetate and Ethinyl Estradiol
Dosage Form Name KIT
Route Name ORAL
Start Marketing Date 20030623
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name
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Complete Information of Zovia 1/35E-28


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