Twynsta - 0597-0125-37 - (telmisartan/amlodipine)

Alphabetical Index


Drug Information of Twynsta

Product NDC: 0597-0125
Proprietary Name: Twynsta
Non Proprietary Name: telmisartan/amlodipine
Active Ingredient(s): 10; 40    mg/1; mg/1 & nbsp;   telmisartan/amlodipine
Administration Route(s): ORAL
Dosage Form(s): TABLET, MULTILAYER
Coding System: National Drug Codes(NDC)

Labeler Information of Twynsta

Product NDC: 0597-0125
Labeler Name: Boehringer Ingelheim Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022401
Marketing Category: NDA
Start Marketing Date: 20091102

Package Information of Twynsta

Package NDC: 0597-0125-37
Package Description: 3 BLISTER PACK in 1 CARTON (0597-0125-37) > 10 TABLET, MULTILAYER in 1 BLISTER PACK

NDC Information of Twynsta

NDC Code 0597-0125-37
Proprietary Name Twynsta
Package Description 3 BLISTER PACK in 1 CARTON (0597-0125-37) > 10 TABLET, MULTILAYER in 1 BLISTER PACK
Product NDC 0597-0125
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name telmisartan/amlodipine
Dosage Form Name TABLET, MULTILAYER
Route Name ORAL
Start Marketing Date 20091102
Marketing Category Name NDA
Labeler Name Boehringer Ingelheim Pharmaceuticals, Inc.
Substance Name AMLODIPINE BESYLATE; TELMISARTAN
Strength Number 10; 40
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Twynsta


General Information