Diovan - 0078-0359-06 - (valsartan)

Alphabetical Index


Drug Information of Diovan

Product NDC: 0078-0359
Proprietary Name: Diovan
Non Proprietary Name: valsartan
Active Ingredient(s): 160    mg/1 & nbsp;   valsartan
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Diovan

Product NDC: 0078-0359
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021283
Marketing Category: NDA
Start Marketing Date: 20010701

Package Information of Diovan

Package NDC: 0078-0359-06
Package Description: 100 BLISTER PACK in 1 BOX (0078-0359-06) > 1 TABLET in 1 BLISTER PACK (0078-0359-61)

NDC Information of Diovan

NDC Code 0078-0359-06
Proprietary Name Diovan
Package Description 100 BLISTER PACK in 1 BOX (0078-0359-06) > 1 TABLET in 1 BLISTER PACK (0078-0359-61)
Product NDC 0078-0359
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name valsartan
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010701
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
Substance Name VALSARTAN
Strength Number 160
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Diovan


General Information