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Sildenafil
Sildenafil - 59762-0033-1 - (SILDENAFIL CITRATE)
Drug Information of Sildenafil
| Product NDC: | 59762-0033 |
| Proprietary Name: | Sildenafil |
| 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) |
Labeler Information of Sildenafil
| Product NDC: | 59762-0033 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021845 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20120927 |
Package Information of Sildenafil
| Package NDC: | 59762-0033-1 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (59762-0033-1) |
NDC Information of Sildenafil
| NDC Code | 59762-0033-1 |
| Proprietary Name | Sildenafil |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (59762-0033-1) |
| Product NDC | 59762-0033 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SILDENAFIL CITRATE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120927 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | SILDENAFIL CITRATE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA] |
