Home > National Drug Code (NDC) > Glyburide and Metformin Hydrochloride

Glyburide and Metformin Hydrochloride - 0228-2752-50 - (Glyburide and Metformin Hydrochloride)

Alphabetical Index


Drug Information of Glyburide and Metformin Hydrochloride

Product NDC: 0228-2752
Proprietary Name: Glyburide and Metformin Hydrochloride
Non Proprietary Name: Glyburide and Metformin Hydrochloride
Active Ingredient(s): 2.5; 500    mg/1; mg/1 & nbsp;   Glyburide and Metformin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glyburide and Metformin Hydrochloride

Product NDC: 0228-2752
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076716
Marketing Category: ANDA
Start Marketing Date: 20050628

Package Information of Glyburide and Metformin Hydrochloride

Package NDC: 0228-2752-50
Package Description: 500 TABLET in 1 BOTTLE (0228-2752-50)

NDC Information of Glyburide and Metformin Hydrochloride

NDC Code 0228-2752-50
Proprietary Name Glyburide and Metformin Hydrochloride
Package Description 500 TABLET in 1 BOTTLE (0228-2752-50)
Product NDC 0228-2752
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glyburide and Metformin Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050628
Marketing Category Name ANDA
Labeler Name Actavis Elizabeth LLC
Substance Name GLYBURIDE; METFORMIN HYDROCHLORIDE
Strength Number 2.5; 500
Strength Unit mg/1; mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient],Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Glyburide and Metformin Hydrochloride


General Information