Product NDC: | 55154-2729 |
Proprietary Name: | Revatio |
Non Proprietary Name: | sildenafil citrate |
Active Ingredient(s): | 20 mg/1 & nbsp; sildenafil citrate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-2729 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021845 |
Marketing Category: | NDA |
Start Marketing Date: | 20050603 |
Package NDC: | 55154-2729-0 |
Package Description: | 10 POUCH in 1 BAG (55154-2729-0) > 1 TABLET, FILM COATED in 1 POUCH |
NDC Code | 55154-2729-0 |
Proprietary Name | Revatio |
Package Description | 10 POUCH in 1 BAG (55154-2729-0) > 1 TABLET, FILM COATED in 1 POUCH |
Product NDC | 55154-2729 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sildenafil citrate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20050603 |
Marketing Category Name | NDA |
Labeler Name | Cardinal Health |
Substance Name | SILDENAFIL CITRATE |
Strength Number | 20 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA] |