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JANUMET
JANUMET - 0006-0081-14 - (sitagliptin and metformin hydrochloride)
Drug Information of JANUMET
| Product NDC: | 0006-0081 |
| Proprietary Name: | JANUMET |
| Non Proprietary Name: | sitagliptin and metformin hydrochloride |
| Active Ingredient(s): | 1000; 100 mg/1; mg/1 & nbsp; sitagliptin and metformin hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of JANUMET
| Product NDC: | 0006-0081 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA202270 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120202 |
Package Information of JANUMET
| Package NDC: | 0006-0081-14 |
| Package Description: | 2 BOTTLE in 1 CARTON (0006-0081-14) > 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0006-0081-07) |
NDC Information of JANUMET
| NDC Code | 0006-0081-14 |
| Proprietary Name | JANUMET |
| Package Description | 2 BOTTLE in 1 CARTON (0006-0081-14) > 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0006-0081-07) |
| Product NDC | 0006-0081 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sitagliptin and metformin hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120202 |
| Marketing Category Name | NDA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE |
| Strength Number | 1000; 100 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Dipeptidyl Peptidase 4 Inhibitor [EPC],Dipeptidyl Peptidase 4 Inhibitors [MoA],Biguanide [EPC],Biguanides [Chemical/Ingredient] |
