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Glipizide and Metformin Hydrochloride - 0378-3133-05 - (glipizide and metformin hydrochloride)

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Drug Information of Glipizide and Metformin Hydrochloride

Product NDC: 0378-3133
Proprietary Name: Glipizide and Metformin Hydrochloride
Non Proprietary Name: glipizide and metformin hydrochloride
Active Ingredient(s): 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: 0378-3133
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078083
Marketing Category: ANDA
Start Marketing Date: 20120503

Package Information of Glipizide and Metformin Hydrochloride

Package NDC: 0378-3133-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3133-05)

NDC Information of Glipizide and Metformin Hydrochloride

NDC Code 0378-3133-05
Proprietary Name Glipizide and Metformin Hydrochloride
Package Description 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3133-05)
Product NDC 0378-3133
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 20120503
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name GLIPIZIDE; METFORMIN HYDROCHLORIDE
Strength Number 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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