Product NDC: | 66302-467 |
Proprietary Name: | ADCIRCA |
Non Proprietary Name: | Tadalafil |
Active Ingredient(s): | 20 mg/1 & nbsp; Tadalafil |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66302-467 |
Labeler Name: | United Therapeutics Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022332 |
Marketing Category: | NDA |
Start Marketing Date: | 20090522 |
Package NDC: | 66302-467-60 |
Package Description: | 60 TABLET in 1 BOTTLE (66302-467-60) |
NDC Code | 66302-467-60 |
Proprietary Name | ADCIRCA |
Package Description | 60 TABLET in 1 BOTTLE (66302-467-60) |
Product NDC | 66302-467 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Tadalafil |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20090522 |
Marketing Category Name | NDA |
Labeler Name | United Therapeutics Corporation |
Substance Name | TADALAFIL |
Strength Number | 20 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA] |