Product NDC: | 54868-4778 |
Proprietary Name: | Zovia 1/50E-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) |
Product NDC: | 54868-4778 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA072723 |
Marketing Category: | ANDA |
Start Marketing Date: | 20030421 |
Package NDC: | 54868-4778-0 |
Package Description: | 1 BLISTER PACK in 1 CONTAINER (54868-4778-0) > 1 KIT in 1 BLISTER PACK |
NDC Code | 54868-4778-0 |
Proprietary Name | Zovia 1/50E-28 |
Package Description | 1 BLISTER PACK in 1 CONTAINER (54868-4778-0) > 1 KIT in 1 BLISTER PACK |
Product NDC | 54868-4778 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ethynodiol Diacetate and Ethinyl Estradiol |
Dosage Form Name | KIT |
Route Name | ORAL |
Start Marketing Date | 20030421 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
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