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FORTAMET
FORTAMET - 59630-575-99 - (metformin hydrochloride)
Drug Information of FORTAMET
| Product NDC: | 59630-575 |
| Proprietary Name: | FORTAMET |
| Non Proprietary Name: | metformin hydrochloride |
| Active Ingredient(s): | 1000 mg/1 & nbsp; metformin hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FORTAMET
| Product NDC: | 59630-575 |
| Labeler Name: | Shionogi Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021574 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040427 |
Package Information of FORTAMET
| Package NDC: | 59630-575-99 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (59630-575-99) > 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of FORTAMET
| NDC Code | 59630-575-99 |
| Proprietary Name | FORTAMET |
| Package Description | 1 BLISTER PACK in 1 CARTON (59630-575-99) > 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 59630-575 |
| 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 | 1000 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |
