Product NDC: | 0006-0112 |
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: | 0006-0112 |
Labeler Name: | Merck Sharp & Dohme Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021995 |
Marketing Category: | NDA |
Start Marketing Date: | 20061016 |
Package NDC: | 0006-0112-31 |
Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (0006-0112-31) |
NDC Code | 0006-0112-31 |
Proprietary Name | JANUVIA |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0006-0112-31) |
Product NDC | 0006-0112 |
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 | Merck Sharp & Dohme Corp. |
Substance Name | SITAGLIPTIN PHOSPHATE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Dipeptidyl Peptidase 4 Inhibitor [EPC],Dipeptidyl Peptidase 4 Inhibitors [MoA] |