Home > National Drug Code (NDC) > Micardis HCT

Micardis HCT - 54868-5297-0 - (TELMISARTAN AND HYDROCHLOROTHIAZIDE)

Alphabetical Index


Drug Information of Micardis HCT

Product NDC: 54868-5297
Proprietary Name: Micardis HCT
Non Proprietary Name: TELMISARTAN AND HYDROCHLOROTHIAZIDE
Active Ingredient(s): 25; 80    mg/1; mg/1 & nbsp;   TELMISARTAN AND HYDROCHLOROTHIAZIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Micardis HCT

Product NDC: 54868-5297
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021162
Marketing Category: NDA
Start Marketing Date: 20050630

Package Information of Micardis HCT

Package NDC: 54868-5297-0
Package Description: 3 BLISTER PACK in 1 CARTON (54868-5297-0) > 10 TABLET in 1 BLISTER PACK

NDC Information of Micardis HCT

NDC Code 54868-5297-0
Proprietary Name Micardis HCT
Package Description 3 BLISTER PACK in 1 CARTON (54868-5297-0) > 10 TABLET in 1 BLISTER PACK
Product NDC 54868-5297
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TELMISARTAN AND HYDROCHLOROTHIAZIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050630
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name HYDROCHLOROTHIAZIDE; TELMISARTAN
Strength Number 25; 80
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Micardis HCT


General Information