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Zenchent FE
Zenchent FE - 52544-292-41 - (Norethindrone and Ethinyl Estradiol)
Drug Information of Zenchent FE
| Product NDC: | 52544-292 |
| Proprietary Name: | Zenchent FE |
| Non Proprietary Name: | Norethindrone and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Norethindrone and Ethinyl Estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zenchent FE
| Product NDC: | 52544-292 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078892 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110926 |
Package Information of Zenchent FE
| Package NDC: | 52544-292-41 |
| Package Description: | 1 KIT in 1 BLISTER PACK (52544-292-41) |
NDC Information of Zenchent FE
| NDC Code | 52544-292-41 |
| Proprietary Name | Zenchent FE |
| Package Description | 1 KIT in 1 BLISTER PACK (52544-292-41) |
| Product NDC | 52544-292 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norethindrone and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110926 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
