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Sildenafil Citrate
Sildenafil Citrate - 68084-622-21 - (Sildenafil Citrate)
Drug Information of Sildenafil Citrate
| Product NDC: | 68084-622 |
| Proprietary Name: | Sildenafil Citrate |
| 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 Citrate
| Product NDC: | 68084-622 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091379 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121214 |
Package Information of Sildenafil Citrate
| Package NDC: | 68084-622-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-622-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-622-11) |
NDC Information of Sildenafil Citrate
| NDC Code | 68084-622-21 |
| Proprietary Name | Sildenafil Citrate |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-622-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-622-11) |
| Product NDC | 68084-622 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sildenafil Citrate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121214 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | SILDENAFIL CITRATE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA] |
