Product NDC: | 52544-248 |
Proprietary Name: | TriNessa |
Non Proprietary Name: | norgestimate and ethinyl estradiol |
Active Ingredient(s): | & nbsp; norgestimate and ethinyl estradiol |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52544-248 |
Labeler Name: | Watson Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019653 |
Marketing Category: | NDA |
Start Marketing Date: | 20030211 |
Package NDC: | 52544-248-28 |
Package Description: | 1 DIALPACK in 1 CARTON (52544-248-28) > 1 KIT in 1 DIALPACK |
NDC Code | 52544-248-28 |
Proprietary Name | TriNessa |
Package Description | 1 DIALPACK in 1 CARTON (52544-248-28) > 1 KIT in 1 DIALPACK |
Product NDC | 52544-248 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | norgestimate and ethinyl estradiol |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20030211 |
Marketing Category Name | NDA |
Labeler Name | Watson Pharmaceuticals |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |