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Riomet
Riomet - 10631-206-01 - (Metformin hydrochloride)
Drug Information of Riomet
| Product NDC: | 10631-206 |
| Proprietary Name: | Riomet |
| Non Proprietary Name: | Metformin hydrochloride |
| Active Ingredient(s): | 500 mg/5mL & nbsp; Metformin hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Riomet
| Product NDC: | 10631-206 |
| Labeler Name: | Ranbaxy Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021591 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040104 |
Package Information of Riomet
| Package NDC: | 10631-206-01 |
| Package Description: | 118 mL in 1 BOTTLE (10631-206-01) |
NDC Information of Riomet
| NDC Code | 10631-206-01 |
| Proprietary Name | Riomet |
| Package Description | 118 mL in 1 BOTTLE (10631-206-01) |
| Product NDC | 10631-206 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metformin hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20040104 |
| Marketing Category Name | NDA |
| Labeler Name | Ranbaxy Laboratories Inc. |
| Substance Name | METFORMIN HYDROCHLORIDE |
| Strength Number | 500 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |
