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Pioglitazone - 0093-2048-05 - (pioglitazone)

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Drug Information of Pioglitazone

Product NDC: 0093-2048
Proprietary Name: Pioglitazone
Non Proprietary Name: pioglitazone
Active Ingredient(s): 15    mg/1 & nbsp;   pioglitazone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pioglitazone

Product NDC: 0093-2048
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021073
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20120817

Package Information of Pioglitazone

Package NDC: 0093-2048-05
Package Description: 500 TABLET in 1 BOTTLE (0093-2048-05)

NDC Information of Pioglitazone

NDC Code 0093-2048-05
Proprietary Name Pioglitazone
Package Description 500 TABLET in 1 BOTTLE (0093-2048-05)
Product NDC 0093-2048
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pioglitazone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120817
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name PIOGLITAZONE HYDROCHLORIDE
Strength Number 15
Strength Unit 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]

Complete Information of Pioglitazone


General Information