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Actoplus Met - 54868-5553-2 - (pioglitazone hydrochloride and metformin hydrochloride)

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Drug Information of Actoplus Met

Product NDC: 54868-5553
Proprietary Name: Actoplus Met
Non Proprietary Name: pioglitazone hydrochloride and metformin hydrochloride
Active Ingredient(s): 850; 15    mg/1; mg/1 & nbsp;   pioglitazone hydrochloride and metformin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Actoplus Met

Product NDC: 54868-5553
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021842
Marketing Category: NDA
Start Marketing Date: 20060321

Package Information of Actoplus Met

Package NDC: 54868-5553-2
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5553-2)

NDC Information of Actoplus Met

NDC Code 54868-5553-2
Proprietary Name Actoplus Met
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5553-2)
Product NDC 54868-5553
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pioglitazone hydrochloride and metformin hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060321
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE
Strength Number 850; 15
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],Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of Actoplus Met


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