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