FORTAMET - 59630-575-99 - (metformin hydrochloride)

Alphabetical Index


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]

Complete Information of FORTAMET


General Information