| Product NDC: | 50102-130 |
| Proprietary Name: | CHATEAL |
| Non Proprietary Name: | Levonorgestrel and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Levonorgestrel and Ethinyl Estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50102-130 |
| Labeler Name: | Afaxys Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091663 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130122 |
| Package NDC: | 50102-130-90 |
| Package Description: | 3 PACKAGE in 1 CASE (50102-130-90) > 48 CARTON in 1 PACKAGE (50102-130-48) > 1 KIT in 1 CARTON (50102-130-01) |
| NDC Code | 50102-130-90 |
| Proprietary Name | CHATEAL |
| Package Description | 3 PACKAGE in 1 CASE (50102-130-90) > 48 CARTON in 1 PACKAGE (50102-130-48) > 1 KIT in 1 CARTON (50102-130-01) |
| Product NDC | 50102-130 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levonorgestrel and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20130122 |
| Marketing Category Name | ANDA |
| Labeler Name | Afaxys Inc. |
| Substance Name | |
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