 
                        | Product NDC: | 55154-5037 | 
| Proprietary Name: | JANUVIA | 
| Non Proprietary Name: | sitagliptin | 
| Active Ingredient(s): | 50 mg/1 & nbsp; sitagliptin | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET, FILM COATED | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 55154-5037 | 
| Labeler Name: | Cardinal Health | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | NDA021995 | 
| Marketing Category: | NDA | 
| Start Marketing Date: | 20061016 | 
| Package NDC: | 55154-5037-7 | 
| Package Description: | 14 TABLET, FILM COATED in 1 BLISTER PACK (55154-5037-7) | 
| NDC Code | 55154-5037-7 | 
| Proprietary Name | JANUVIA | 
| Package Description | 14 TABLET, FILM COATED in 1 BLISTER PACK (55154-5037-7) | 
| Product NDC | 55154-5037 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | sitagliptin | 
| Dosage Form Name | TABLET, FILM COATED | 
| Route Name | ORAL | 
| Start Marketing Date | 20061016 | 
| Marketing Category Name | NDA | 
| Labeler Name | Cardinal Health | 
| Substance Name | SITAGLIPTIN PHOSPHATE | 
| Strength Number | 50 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Dipeptidyl Peptidase 4 Inhibitor [EPC],Dipeptidyl Peptidase 4 Inhibitors [MoA] |