JANUMET - 35356-136-60 - (sitagliptin and metformin hydrochloride)

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Drug Information of JANUMET

Product NDC: 35356-136
Proprietary Name: JANUMET
Non Proprietary Name: sitagliptin and metformin hydrochloride
Active Ingredient(s): 500; 50    mg/1; mg/1 & nbsp;   sitagliptin and metformin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of JANUMET

Product NDC: 35356-136
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022044
Marketing Category: NDA
Start Marketing Date: 20120309

Package Information of JANUMET

Package NDC: 35356-136-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (35356-136-60)

NDC Information of JANUMET

NDC Code 35356-136-60
Proprietary Name JANUMET
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (35356-136-60)
Product NDC 35356-136
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sitagliptin and metformin hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120309
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE
Strength Number 500; 50
Strength Unit mg/1; mg/1
Pharmaceutical Classes Dipeptidyl Peptidase 4 Inhibitor [EPC],Dipeptidyl Peptidase 4 Inhibitors [MoA],Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of JANUMET


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