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PrandiMet
PrandiMet - 0169-0093-21 - (repaglinide and metformin hydrochloride)
Drug Information of PrandiMet
| Product NDC: | 0169-0093 |
| Proprietary Name: | PrandiMet |
| Non Proprietary Name: | repaglinide and metformin hydrochloride |
| Active Ingredient(s): | 500; 1 mg/1; mg/1 & nbsp; repaglinide and metformin hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PrandiMet
| Product NDC: | 0169-0093 |
| Labeler Name: | Novo Nordisk |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022386 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090116 |
Package Information of PrandiMet
| Package NDC: | 0169-0093-21 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0169-0093-21) > 20 TABLET in 1 BOTTLE, PLASTIC |
NDC Information of PrandiMet
| NDC Code | 0169-0093-21 |
| Proprietary Name | PrandiMet |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0169-0093-21) > 20 TABLET in 1 BOTTLE, PLASTIC |
| Product NDC | 0169-0093 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | repaglinide and metformin hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090116 |
| Marketing Category Name | NDA |
| Labeler Name | Novo Nordisk |
| Substance Name | METFORMIN HYDROCHLORIDE; REPAGLINIDE |
| Strength Number | 500; 1 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Glinide [EPC],Potassium Channel Antagonists [MoA],Biguanide [EPC],Biguanides [Chemical/Ingredient] |
