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Glipizide and Metformin Hydrochloride - 54868-5188-0 - (Glipizide and Metformin Hydrochloride)

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Drug Information of Glipizide and Metformin Hydrochloride

Product NDC: 54868-5188
Proprietary Name: Glipizide and Metformin Hydrochloride
Non Proprietary Name: Glipizide and Metformin Hydrochloride
Active Ingredient(s): 2.5; 500    mg/1; mg/1 & nbsp;   Glipizide and Metformin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Glipizide and Metformin Hydrochloride

Product NDC: 54868-5188
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077270
Marketing Category: ANDA
Start Marketing Date: 20051114

Package Information of Glipizide and Metformin Hydrochloride

Package NDC: 54868-5188-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-5188-0)

NDC Information of Glipizide and Metformin Hydrochloride

NDC Code 54868-5188-0
Proprietary Name Glipizide and Metformin Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-5188-0)
Product NDC 54868-5188
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide and Metformin Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20051114
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name GLIPIZIDE; 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 Glipizide and Metformin Hydrochloride


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