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Glipizide and Metformin Hydrochloride - 0093-7455-01 - (Glipizide and Metformin Hydrochloride)

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Drug Information of Glipizide and Metformin Hydrochloride

Product NDC: 0093-7455
Proprietary Name: Glipizide and Metformin Hydrochloride
Non Proprietary Name: Glipizide and Metformin Hydrochloride
Active Ingredient(s): 2.5; 250    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: 0093-7455
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077270
Marketing Category: ANDA
Start Marketing Date: 20051028

Package Information of Glipizide and Metformin Hydrochloride

Package NDC: 0093-7455-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0093-7455-01)

NDC Information of Glipizide and Metformin Hydrochloride

NDC Code 0093-7455-01
Proprietary Name Glipizide and Metformin Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0093-7455-01)
Product NDC 0093-7455
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 20051028
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name GLIPIZIDE; METFORMIN HYDROCHLORIDE
Strength Number 2.5; 250
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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