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Glyburide and Metformin - 54868-5185-3 - (Glyburide and Metformin)

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Drug Information of Glyburide and Metformin

Product NDC: 54868-5185
Proprietary Name: Glyburide and Metformin
Non Proprietary Name: Glyburide and Metformin
Active Ingredient(s): 1.25; 250    mg/1; mg/1 & nbsp;   Glyburide and Metformin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Glyburide and Metformin

Product NDC: 54868-5185
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076345
Marketing Category: ANDA
Start Marketing Date: 20041119

Package Information of Glyburide and Metformin

Package NDC: 54868-5185-3
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-5185-3)

NDC Information of Glyburide and Metformin

NDC Code 54868-5185-3
Proprietary Name Glyburide and Metformin
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-5185-3)
Product NDC 54868-5185
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glyburide and Metformin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20041119
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name GLYBURIDE; METFORMIN HYDROCHLORIDE
Strength Number 1.25; 250
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


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