Diovan - 21695-917-90 - (valsartan)

Alphabetical Index


Drug Information of Diovan

Product NDC: 21695-917
Proprietary Name: Diovan
Non Proprietary Name: valsartan
Active Ingredient(s): 80    mg/1 & nbsp;   valsartan
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Diovan

Product NDC: 21695-917
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021283
Marketing Category: NDA
Start Marketing Date: 20010701

Package Information of Diovan

Package NDC: 21695-917-90
Package Description: 90 TABLET in 1 BOTTLE (21695-917-90)

NDC Information of Diovan

NDC Code 21695-917-90
Proprietary Name Diovan
Package Description 90 TABLET in 1 BOTTLE (21695-917-90)
Product NDC 21695-917
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 Rebel Distributors Corp
Substance Name VALSARTAN
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Diovan


General Information