Micardis - 54868-6193-0 - (TELMISARTAN)

Alphabetical Index


Drug Information of Micardis

Product NDC: 54868-6193
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: 54868-6193
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020850
Marketing Category: NDA
Start Marketing Date: 20101102

Package Information of Micardis

Package NDC: 54868-6193-0
Package Description: 3 BLISTER PACK in 1 CARTON (54868-6193-0) > 10 TABLET in 1 BLISTER PACK

NDC Information of Micardis

NDC Code 54868-6193-0
Proprietary Name Micardis
Package Description 3 BLISTER PACK in 1 CARTON (54868-6193-0) > 10 TABLET in 1 BLISTER PACK
Product NDC 54868-6193
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TELMISARTAN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101102
Marketing Category Name NDA
Labeler Name Physicians Total Care, 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