| Product NDC: | 54868-5558 |
| Proprietary Name: | Fortamet |
| Non Proprietary Name: | metformin hydrochloride |
| Active Ingredient(s): | 500 mg/1 & nbsp; metformin hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54868-5558 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021574 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060324 |
| Package NDC: | 54868-5558-0 |
| Package Description: | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-5558-0) |
| NDC Code | 54868-5558-0 |
| Proprietary Name | Fortamet |
| Package Description | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-5558-0) |
| Product NDC | 54868-5558 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | metformin hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20060324 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | METFORMIN HYDROCHLORIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |