Home > National Drug Code (NDC) > Actoplus Met

Actoplus Met - 54868-5500-0 - (pioglitazone hydrochloride and metformin hydrochloride)

Alphabetical Index


Drug Information of Actoplus Met

Product NDC: 54868-5500
Proprietary Name: Actoplus Met
Non Proprietary Name: pioglitazone hydrochloride and metformin hydrochloride
Active Ingredient(s): 500; 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: 54868-5500
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021842
Marketing Category: NDA
Start Marketing Date: 20060104

Package Information of Actoplus Met

Package NDC: 54868-5500-0
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5500-0)

NDC Information of Actoplus Met

NDC Code 54868-5500-0
Proprietary Name Actoplus Met
Package Description 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5500-0)
Product NDC 54868-5500
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 20060104
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE
Strength Number 500; 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


General Information