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Pioglitazone Hydrochloride - 68084-629-01 - (pioglitazone hydrochloride)

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Drug Information of Pioglitazone Hydrochloride

Product NDC: 68084-629
Proprietary Name: Pioglitazone Hydrochloride
Non Proprietary Name: pioglitazone hydrochloride
Active Ingredient(s): 15    mg/1 & nbsp;   pioglitazone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pioglitazone Hydrochloride

Product NDC: 68084-629
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021073
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20130625

Package Information of Pioglitazone Hydrochloride

Package NDC: 68084-629-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-629-01) > 10 TABLET in 1 BLISTER PACK (68084-629-11)

NDC Information of Pioglitazone Hydrochloride

NDC Code 68084-629-01
Proprietary Name Pioglitazone Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (68084-629-01) > 10 TABLET in 1 BLISTER PACK (68084-629-11)
Product NDC 68084-629
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pioglitazone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130625
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name American Health Packaging
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 Hydrochloride


General Information