Product NDC: | 49999-316 |
Proprietary Name: | Viagra |
Non Proprietary Name: | sildenafil citrate |
Active Ingredient(s): | 100 mg/1 & nbsp; sildenafil citrate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49999-316 |
Labeler Name: | Lake Erie Medical Surgical & Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020895 |
Marketing Category: | NDA |
Start Marketing Date: | 20110713 |
Package NDC: | 49999-316-15 |
Package Description: | 15 TABLET, FILM COATED in 1 BOTTLE (49999-316-15) |
NDC Code | 49999-316-15 |
Proprietary Name | Viagra |
Package Description | 15 TABLET, FILM COATED in 1 BOTTLE (49999-316-15) |
Product NDC | 49999-316 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sildenafil citrate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20110713 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical Surgical & Supply DBA Quality Care Products LLC |
Substance Name | SILDENAFIL CITRATE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA] |