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PIOGLITAZONEHYDROCHLORIDE - 13668-119-05 - (PIOGLITAZONEHYDROCHLORIDE)

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Drug Information of PIOGLITAZONEHYDROCHLORIDE

Product NDC: 13668-119
Proprietary Name: PIOGLITAZONEHYDROCHLORIDE
Non Proprietary Name: PIOGLITAZONEHYDROCHLORIDE
Active Ingredient(s): 30    mg/1 & nbsp;   PIOGLITAZONEHYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PIOGLITAZONEHYDROCHLORIDE

Product NDC: 13668-119
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091298
Marketing Category: ANDA
Start Marketing Date: 20130213

Package Information of PIOGLITAZONEHYDROCHLORIDE

Package NDC: 13668-119-05
Package Description: 500 TABLET in 1 BOTTLE (13668-119-05)

NDC Information of PIOGLITAZONEHYDROCHLORIDE

NDC Code 13668-119-05
Proprietary Name PIOGLITAZONEHYDROCHLORIDE
Package Description 500 TABLET in 1 BOTTLE (13668-119-05)
Product NDC 13668-119
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PIOGLITAZONEHYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130213
Marketing Category Name ANDA
Labeler Name Torrent Pharmaceuticals Limited
Substance Name PIOGLITAZONE HYDROCHLORIDE
Strength Number 30
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 PIOGLITAZONEHYDROCHLORIDE


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