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CIALIS
CIALIS - 16590-905-10 - (TADALAFIL)
Drug Information of CIALIS
| Product NDC: | 16590-905 |
| Proprietary Name: | CIALIS |
| Non Proprietary Name: | TADALAFIL |
| Active Ingredient(s): | 10 mg/1 & nbsp; TADALAFIL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CIALIS
| Product NDC: | 16590-905 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021368 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20031126 |
Package Information of CIALIS
| Package NDC: | 16590-905-10 |
| Package Description: | 10 TABLET, FILM COATED in 1 BOTTLE (16590-905-10) |
NDC Information of CIALIS
| NDC Code | 16590-905-10 |
| Proprietary Name | CIALIS |
| Package Description | 10 TABLET, FILM COATED in 1 BOTTLE (16590-905-10) |
| Product NDC | 16590-905 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TADALAFIL |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20031126 |
| Marketing Category Name | NDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | TADALAFIL |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA] |
