Home > National Drug Code (NDC) > Metformin Hydrochloride

Metformin Hydrochloride - 43547-322-11 - (Metformin Hydrochloride)

Alphabetical Index


Drug Information of Metformin Hydrochloride

Product NDC: 43547-322
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Metformin Hydrochloride

Product NDC: 43547-322
Labeler Name: Solco healthcare U.S., LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090888
Marketing Category: ANDA
Start Marketing Date: 20130415

Package Information of Metformin Hydrochloride

Package NDC: 43547-322-11
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (43547-322-11)

NDC Information of Metformin Hydrochloride

NDC Code 43547-322-11
Proprietary Name Metformin Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (43547-322-11)
Product NDC 43547-322
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metformin Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130415
Marketing Category Name ANDA
Labeler Name Solco healthcare U.S., LLC
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