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) |
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 NDC: | 10631-206-02 |
Package Description: | 473 mL in 1 BOTTLE (10631-206-02) |
NDC Code | 10631-206-02 |
Proprietary Name | Riomet |
Package Description | 473 mL in 1 BOTTLE (10631-206-02) |
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] |