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Micardis HCT - 0597-0044-37 - (telmisartan and hydrochlorothiazide)

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Drug Information of Micardis HCT

Product NDC: 0597-0044
Proprietary Name: Micardis HCT
Non Proprietary Name: telmisartan and hydrochlorothiazide
Active Ingredient(s): 12.5; 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: 0597-0044
Labeler Name: Boehringer Ingelheim Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021162
Marketing Category: NDA
Start Marketing Date: 20001201

Package Information of Micardis HCT

Package NDC: 0597-0044-37
Package Description: 3 BLISTER PACK in 1 CARTON (0597-0044-37) > 10 TABLET in 1 BLISTER PACK

NDC Information of Micardis HCT

NDC Code 0597-0044-37
Proprietary Name Micardis HCT
Package Description 3 BLISTER PACK in 1 CARTON (0597-0044-37) > 10 TABLET in 1 BLISTER PACK
Product NDC 0597-0044
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name telmisartan and hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20001201
Marketing Category Name NDA
Labeler Name Boehringer Ingelheim Pharmaceuticals, Inc.
Substance Name HYDROCHLOROTHIAZIDE; TELMISARTAN
Strength Number 12.5; 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


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