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Pioglitazone - 0378-0228-93 - (pioglitazone)

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Drug Information of Pioglitazone

Product NDC: 0378-0228
Proprietary Name: Pioglitazone
Non Proprietary Name: pioglitazone
Active Ingredient(s): 30    mg/1 & nbsp;   pioglitazone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pioglitazone

Product NDC: 0378-0228
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076801
Marketing Category: ANDA
Start Marketing Date: 20120817

Package Information of Pioglitazone

Package NDC: 0378-0228-93
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (0378-0228-93)

NDC Information of Pioglitazone

NDC Code 0378-0228-93
Proprietary Name Pioglitazone
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (0378-0228-93)
Product NDC 0378-0228
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pioglitazone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120817
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
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 Pioglitazone


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