| Product NDC: | 66336-566 | 
| Proprietary Name: | Cialis | 
| Non Proprietary Name: | Tadalafil | 
| Active Ingredient(s): | 20 mg/1 & nbsp; Tadalafil | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET, FILM COATED | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 66336-566 | 
| Labeler Name: | Dispensing Solutions, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | NDA021368 | 
| Marketing Category: | NDA | 
| Start Marketing Date: | 20031126 | 
| Package NDC: | 66336-566-05 | 
| Package Description: | 5 TABLET, FILM COATED in 1 BOTTLE (66336-566-05) | 
| NDC Code | 66336-566-05 | 
| Proprietary Name | Cialis | 
| Package Description | 5 TABLET, FILM COATED in 1 BOTTLE (66336-566-05) | 
| Product NDC | 66336-566 | 
| 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 | Dispensing Solutions, Inc. | 
| Substance Name | TADALAFIL | 
| Strength Number | 20 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA] |