Home > National Drug Code (NDC) > Metformin Hydrochloride

Metformin Hydrochloride - 52125-354-02 - (Metformin Hydrochloride)

Alphabetical Index


Drug Information of Metformin Hydrochloride

Product NDC: 52125-354
Proprietary Name: Metformin Hydrochloride
Non Proprietary Name: Metformin Hydrochloride
Active Ingredient(s): 850    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: 52125-354
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078170
Marketing Category: ANDA
Start Marketing Date: 20130528

Package Information of Metformin Hydrochloride

Package NDC: 52125-354-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-354-02)

NDC Information of Metformin Hydrochloride

NDC Code 52125-354-02
Proprietary Name Metformin Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (52125-354-02)
Product NDC 52125-354
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130528
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 850
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Metformin Hydrochloride


General Information