Home > National Drug Code (NDC) > Metformin Hydrochloride

Metformin Hydrochloride - 54868-4566-3 - (metformin hydrochloride)

Alphabetical Index


Drug Information of Metformin Hydrochloride

Product NDC: 54868-4566
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: metformin hydrochloride
Active Ingredient(s): 1000    mg/1 & nbsp;   metformin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride

Product NDC: 54868-4566
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075967
Marketing Category: ANDA
Start Marketing Date: 20020311

Package Information of Metformin Hydrochloride

Package NDC: 54868-4566-3
Package Description: 90 TABLET in 1 BOTTLE (54868-4566-3)

NDC Information of Metformin Hydrochloride

NDC Code 54868-4566-3
Proprietary Name Metformin Hydrochloride
Package Description 90 TABLET in 1 BOTTLE (54868-4566-3)
Product NDC 54868-4566
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metformin hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020311
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 1000
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


General Information