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Pioglitazone - 0781-5422-10 - (pioglitazone)

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Drug Information of Pioglitazone

Product NDC: 0781-5422
Proprietary Name: Pioglitazone
Non Proprietary Name: pioglitazone
Active Ingredient(s): 45    mg/1 & nbsp;   pioglitazone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pioglitazone

Product NDC: 0781-5422
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078670
Marketing Category: ANDA
Start Marketing Date: 20130301

Package Information of Pioglitazone

Package NDC: 0781-5422-10
Package Description: 1000 TABLET in 1 BOTTLE (0781-5422-10)

NDC Information of Pioglitazone

NDC Code 0781-5422-10
Proprietary Name Pioglitazone
Package Description 1000 TABLET in 1 BOTTLE (0781-5422-10)
Product NDC 0781-5422
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pioglitazone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130301
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name PIOGLITAZONE HYDROCHLORIDE
Strength Number 45
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


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