Product NDC: | 59630-574 |
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, FILM COATED, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59630-574 |
Labeler Name: | Shionogi Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021574 |
Marketing Category: | NDA |
Start Marketing Date: | 20040427 |
Package NDC: | 59630-574-60 |
Package Description: | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (59630-574-60) |
NDC Code | 59630-574-60 |
Proprietary Name | FORTAMET |
Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (59630-574-60) |
Product NDC | 59630-574 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | metformin hydrochloride |
Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20040427 |
Marketing Category Name | NDA |
Labeler Name | Shionogi Inc. |
Substance Name | METFORMIN HYDROCHLORIDE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |