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Pioglitazone and Metformin Hydrocholride - 0093-5050-86 - (pioglitazone and metformin hydrochloride)

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Drug Information of Pioglitazone and Metformin Hydrocholride

Product NDC: 0093-5050
Proprietary Name: Pioglitazone and Metformin Hydrocholride
Non Proprietary Name: pioglitazone and metformin hydrochloride
Active Ingredient(s): 850; 15    mg/1; mg/1 & nbsp;   pioglitazone and metformin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Pioglitazone and Metformin Hydrocholride

Product NDC: 0093-5050
Labeler Name: Teva Pharmaceuticals USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021842
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20120817

Package Information of Pioglitazone and Metformin Hydrocholride

Package NDC: 0093-5050-86
Package Description: 180 TABLET, FILM COATED in 1 BOTTLE (0093-5050-86)

NDC Information of Pioglitazone and Metformin Hydrocholride

NDC Code 0093-5050-86
Proprietary Name Pioglitazone and Metformin Hydrocholride
Package Description 180 TABLET, FILM COATED in 1 BOTTLE (0093-5050-86)
Product NDC 0093-5050
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pioglitazone and metformin hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120817
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Teva Pharmaceuticals USA
Substance Name METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE
Strength Number 850; 15
Strength Unit mg/1; mg/1
Pharmaceutical Classes Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator Receptor gamma Agonist [EPC],Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR alpha [Chemical/Ingredient],PPAR gamma [Chemical/Ingredient],Thiazolidinedione [EPC],Thiazolidinediones [Chemical/Ingredient],Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Pioglitazone and Metformin Hydrocholride


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