Micardis - 0597-0039-37 - (telmisartan)

Alphabetical Index


Drug Information of Micardis

Product NDC: 0597-0039
Proprietary Name: Micardis
Non Proprietary Name: telmisartan
Active Ingredient(s): 20    mg/1 & nbsp;   telmisartan
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Micardis

Product NDC: 0597-0039
Labeler Name: Boehringer Ingelheim Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020850
Marketing Category: NDA
Start Marketing Date: 20001201

Package Information of Micardis

Package NDC: 0597-0039-37
Package Description: 3 BLISTER PACK in 1 CARTON (0597-0039-37) > 10 TABLET in 1 BLISTER PACK

NDC Information of Micardis

NDC Code 0597-0039-37
Proprietary Name Micardis
Package Description 3 BLISTER PACK in 1 CARTON (0597-0039-37) > 10 TABLET in 1 BLISTER PACK
Product NDC 0597-0039
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name telmisartan
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20001201
Marketing Category Name NDA
Labeler Name Boehringer Ingelheim Pharmaceuticals, Inc.
Substance Name TELMISARTAN
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Micardis


General Information