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Pioglitazone - 55648-978-03 - (Pioglitazone)

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Drug Information of Pioglitazone

Product NDC: 55648-978
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: 55648-978
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078038
Marketing Category: ANDA
Start Marketing Date: 20130213

Package Information of Pioglitazone

Package NDC: 55648-978-03
Package Description: 500 TABLET in 1 BOTTLE (55648-978-03)

NDC Information of Pioglitazone

NDC Code 55648-978-03
Proprietary Name Pioglitazone
Package Description 500 TABLET in 1 BOTTLE (55648-978-03)
Product NDC 55648-978
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pioglitazone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130213
Marketing Category Name ANDA
Labeler Name Wockhardt Limited
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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