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Pioglitazone hydrochloride and glimepiride - 0781-5635-06 - (Pioglitazone hydrochloride and glimepiride)

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Drug Information of Pioglitazone hydrochloride and glimepiride

Product NDC: 0781-5635
Proprietary Name: Pioglitazone hydrochloride and glimepiride
Non Proprietary Name: Pioglitazone hydrochloride and glimepiride
Active Ingredient(s): 4; 30    mg/1; mg/1 & nbsp;   Pioglitazone hydrochloride and glimepiride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pioglitazone hydrochloride and glimepiride

Product NDC: 0781-5635
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201049
Marketing Category: ANDA
Start Marketing Date: 20130108

Package Information of Pioglitazone hydrochloride and glimepiride

Package NDC: 0781-5635-06
Package Description: 7 CARTON in 1 BLISTER PACK (0781-5635-06) > 28 TABLET in 1 CARTON (0781-5635-08)

NDC Information of Pioglitazone hydrochloride and glimepiride

NDC Code 0781-5635-06
Proprietary Name Pioglitazone hydrochloride and glimepiride
Package Description 7 CARTON in 1 BLISTER PACK (0781-5635-06) > 28 TABLET in 1 CARTON (0781-5635-08)
Product NDC 0781-5635
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pioglitazone hydrochloride and glimepiride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130108
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE
Strength Number 4; 30
Strength Unit mg/1; 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],Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Pioglitazone hydrochloride and glimepiride


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