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Glipizide and Metformin Hydrochloride - 42291-305-01 - (Glipizide and Metformin Hydrochloride)

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Drug Information of Glipizide and Metformin Hydrochloride

Product NDC: 42291-305
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: 42291-305
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077270
Marketing Category: ANDA
Start Marketing Date: 20130708

Package Information of Glipizide and Metformin Hydrochloride

Package NDC: 42291-305-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (42291-305-01)

NDC Information of Glipizide and Metformin Hydrochloride

NDC Code 42291-305-01
Proprietary Name Glipizide and Metformin Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (42291-305-01)
Product NDC 42291-305
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 20130708
Marketing Category Name ANDA
Labeler Name AvKARE, 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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