DIOVAN HCT - 16590-312-30 - (HYDROCHLOROTHIAZIDE, VALSARTAN)

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Drug Information of DIOVAN HCT

Product NDC: 16590-312
Proprietary Name: DIOVAN HCT
Non Proprietary Name: HYDROCHLOROTHIAZIDE, VALSARTAN
Active Ingredient(s): 12.5; 80    mg/1; mg/1 & nbsp;   HYDROCHLOROTHIAZIDE, VALSARTAN
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of DIOVAN HCT

Product NDC: 16590-312
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020818
Marketing Category: NDA
Start Marketing Date: 20060428

Package Information of DIOVAN HCT

Package NDC: 16590-312-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16590-312-30)

NDC Information of DIOVAN HCT

NDC Code 16590-312-30
Proprietary Name DIOVAN HCT
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16590-312-30)
Product NDC 16590-312
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCHLOROTHIAZIDE, VALSARTAN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060428
Marketing Category Name NDA
Labeler Name STAT RX USA LLC
Substance Name HYDROCHLOROTHIAZIDE; VALSARTAN
Strength Number 12.5; 80
Strength Unit mg/1; mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of DIOVAN HCT


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