Home
>
National Drug Code (NDC)
>
Zovia 1/35E-28
Zovia 1/35E-28 - 52544-383-31 - (Ethynodiol Diacetate and Ethinyl Estradiol)
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: | 52544-383-31 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (52544-383-31) > 1 KIT in 1 BLISTER PACK |
NDC Information of Zovia 1/35E-28
| NDC Code | 52544-383-31 |
| Proprietary Name | Zovia 1/35E-28 |
| Package Description | 3 BLISTER PACK in 1 CARTON (52544-383-31) > 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. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
