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Janumet
Janumet - 54868-1097-1 - (sitagliptin and metformin hydrochloride)
Drug Information of Janumet
| Product NDC: | 54868-1097 |
| Proprietary Name: | Janumet |
| Non Proprietary Name: | sitagliptin and metformin hydrochloride |
| Active Ingredient(s): | 1000; 50 mg/1; mg/1 & nbsp; sitagliptin and metformin hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Janumet
| Product NDC: | 54868-1097 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022044 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080617 |
Package Information of Janumet
| Package NDC: | 54868-1097-1 |
| Package Description: | 180 TABLET, FILM COATED in 1 BOTTLE (54868-1097-1) |
NDC Information of Janumet
| NDC Code | 54868-1097-1 |
| Proprietary Name | Janumet |
| Package Description | 180 TABLET, FILM COATED in 1 BOTTLE (54868-1097-1) |
| Product NDC | 54868-1097 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sitagliptin and metformin hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20080617 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE |
| Strength Number | 1000; 50 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Dipeptidyl Peptidase 4 Inhibitor [EPC],Dipeptidyl Peptidase 4 Inhibitors [MoA],Biguanide [EPC],Biguanides [Chemical/Ingredient] |
