FDA Application Number: 020895 (001)
| Proprietary Name | VIAGRA |
|---|---|
| Active Ingredient | SILDENAFIL CITRATE |
| Applicant | Viatris |
| Route / Dosage form | TABLET;ORAL |
| Strength | EQ 25MG BASE |
| Prescription / OTC | Prescription |
| Date of approval | 27 Mar 1998 |
| Reference listed drug | Yes |
| TE code | AB |
FDA Application Number: 020895 (002)
| Proprietary Name | VIAGRA |
|---|---|
| Active Ingredient | SILDENAFIL CITRATE |
| Applicant | Viatris |
| Route / Dosage form | TABLET;ORAL |
| Strength | EQ 50MG BASE |
| Prescription / OTC | Prescription |
| Date of approval | 27 Mar 1998 |
| Reference listed drug | Yes |
| TE code | AB |
FDA Application Number: 020895 (003)
| Proprietary Name | VIAGRA |
|---|---|
| Active Ingredient | SILDENAFIL CITRATE |
| Applicant | Viatris |
| Route / Dosage form | TABLET;ORAL |
| Strength | EQ 100MG BASE |
| Prescription / OTC | Prescription |
| Date of approval | 27 Mar 1998 |
| Reference listed drug | Yes |
| TE code | AB |