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 | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |