| NDC Code | 0078-0383-17 | 
|---|
			| Package Description | 7000 TABLET, FILM COATED in 1 BOTTLE (0078-0383-17) | 
|---|
			| Product NDC | 0078-0383 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Diovan Hct | 
|---|
			
			| Non-Proprietary Name | Valsartan And Hydrochlorothiazide | 
|---|
			| Dosage Form | TABLET, FILM COATED | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 19980306 | 
|---|
			
			| Marketing Category Name | NDA | 
|---|
			| Application Number | NDA020818 | 
|---|
			| Manufacturer | Novartis Pharmaceuticals Corporation | 
|---|
			| Substance Name | HYDROCHLOROTHIAZIDE; VALSARTAN | 
|---|
			| Strength | 25; 160 | 
|---|
			| Strength Unit | mg/1; mg/1 | 
|---|
			| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] | 
|---|