Nesina - 64764-250-90 - (alogliptin)

Alphabetical Index


Drug Information of Nesina

Product NDC: 64764-250
Proprietary Name: Nesina
Non Proprietary Name: alogliptin
Active Ingredient(s): 25    mg/1 & nbsp;   alogliptin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Nesina

Product NDC: 64764-250
Labeler Name: Takeda Pharmaceuticals America, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022271
Marketing Category: NDA
Start Marketing Date: 20130125

Package Information of Nesina

Package NDC: 64764-250-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (64764-250-90)

NDC Information of Nesina

NDC Code 64764-250-90
Proprietary Name Nesina
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (64764-250-90)
Product NDC 64764-250
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alogliptin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130125
Marketing Category Name NDA
Labeler Name Takeda Pharmaceuticals America, Inc.
Substance Name ALOGLIPTIN BENZOATE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Nesina


General Information