Home > National Drug Code (NDC) > Metformin Hydrochloride

Metformin Hydrochloride - 55154-1376-0 - (Metformin Hydrochloride)

Alphabetical Index


Drug Information of Metformin Hydrochloride

Product NDC: 55154-1376
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: Metformin Hydrochloride
Active Ingredient(s): 500    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: 55154-1376
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077880
Marketing Category: ANDA
Start Marketing Date: 20100111

Package Information of Metformin Hydrochloride

Package NDC: 55154-1376-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-1376-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Metformin Hydrochloride

NDC Code 55154-1376-0
Proprietary Name Metformin Hydrochloride
Package Description 10 BLISTER PACK in 1 BAG (55154-1376-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-1376
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100111
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


General Information