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Glipizide and Metformin HCl - 23155-116-10 - (Glipizide and Metformin HCl)

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Drug Information of Glipizide and Metformin HCl

Product NDC: 23155-116
Proprietary Name: Glipizide and Metformin HCl
Non Proprietary Name: Glipizide and Metformin HCl
Active Ingredient(s): 2.5; 500    mg/1; mg/1 & nbsp;   Glipizide and Metformin HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Glipizide and Metformin HCl

Product NDC: 23155-116
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078728
Marketing Category: ANDA
Start Marketing Date: 20100629

Package Information of Glipizide and Metformin HCl

Package NDC: 23155-116-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (23155-116-10)

NDC Information of Glipizide and Metformin HCl

NDC Code 23155-116-10
Proprietary Name Glipizide and Metformin HCl
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (23155-116-10)
Product NDC 23155-116
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide and Metformin HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100629
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals 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 HCl


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