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Teveten HCT - 0074-3015-11 - (Eprosartan Mesylate and Hydrochlorothiazide)

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Drug Information of Teveten HCT

Product NDC: 0074-3015
Proprietary Name: Teveten HCT
Non Proprietary Name: Eprosartan Mesylate and Hydrochlorothiazide
Active Ingredient(s): 600; 12.5    mg/1; mg/1 & nbsp;   Eprosartan Mesylate and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Teveten HCT

Product NDC: 0074-3015
Labeler Name: Abbott Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021268
Marketing Category: NDA
Start Marketing Date: 20100524

Package Information of Teveten HCT

Package NDC: 0074-3015-11
Package Description: 100 TABLET in 1 BOTTLE (0074-3015-11)

NDC Information of Teveten HCT

NDC Code 0074-3015-11
Proprietary Name Teveten HCT
Package Description 100 TABLET in 1 BOTTLE (0074-3015-11)
Product NDC 0074-3015
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Eprosartan Mesylate and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100524
Marketing Category Name NDA
Labeler Name Abbott Laboratories
Substance Name EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE
Strength Number 600; 12.5
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 Teveten HCT


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