Fortamet - 54868-5558-0 - (metformin hydrochloride)

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Drug Information of Fortamet

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)

Labeler Information of Fortamet

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 Information of Fortamet

Package NDC: 54868-5558-0
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-5558-0)

NDC Information of Fortamet

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]

Complete Information of Fortamet


General Information