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Glyburide and Metformin Hydrochloride - 64720-141-10 - (Glyburide and Metformin Hydrochloride)

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Drug Information of Glyburide and Metformin Hydrochloride

Product NDC: 64720-141
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Glyburide and Metformin Hydrochloride

Product NDC: 64720-141
Labeler Name: CorePharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076731
Marketing Category: ANDA
Start Marketing Date: 20041119

Package Information of Glyburide and Metformin Hydrochloride

Package NDC: 64720-141-10
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64720-141-10)

NDC Information of Glyburide and Metformin Hydrochloride

NDC Code 64720-141-10
Proprietary Name Glyburide and Metformin Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64720-141-10)
Product NDC 64720-141
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glyburide and Metformin Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20041119
Marketing Category Name ANDA
Labeler Name CorePharma, 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


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