Product NDC: | 0781-5583 |
Proprietary Name: | ALTAVERA |
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: | 0781-5583 |
Labeler Name: | Sandoz Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA079102 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100803 |
Package NDC: | 0781-5583-15 |
Package Description: | 3 CARTON in 1 BOX (0781-5583-15) > 1 KIT in 1 CARTON |
NDC Code | 0781-5583-15 |
Proprietary Name | ALTAVERA |
Package Description | 3 CARTON in 1 BOX (0781-5583-15) > 1 KIT in 1 CARTON |
Product NDC | 0781-5583 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Levonorgestrel and Ethinyl Estradiol |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20100803 |
Marketing Category Name | ANDA |
Labeler Name | Sandoz Inc |
Substance Name | |
Strength Number | |
Strength Unit | |
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