-
Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations
Search results from the "OB_Rx" table for query
on "020818."
| Active Ingredient: | HYDROCHLOROTHIAZIDE; VALSARTAN |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | DIOVAN HCT |
| Applicant: | NOVARTIS |
| Strength: | 12.5MG;80MG |
| Application Number: | N020818 |
| Product Number: | 001 |
| Approval Date: | Mar 6, 1998 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | |
| Patent and Exclusivity Info for this product: | View |
|
|
|
| Active Ingredient: | HYDROCHLOROTHIAZIDE; VALSARTAN |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | DIOVAN HCT |
| Applicant: | NOVARTIS |
| Strength: | 12.5MG;160MG |
| Application Number: | N020818 |
| Product Number: | 002 |
| Approval Date: | Mar 6, 1998 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | |
| Patent and Exclusivity Info for this product: | View |
|
|
|
| Active Ingredient: | HYDROCHLOROTHIAZIDE; VALSARTAN |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | DIOVAN HCT |
| Applicant: | NOVARTIS |
| Strength: | 25MG;160MG |
| Application Number: | N020818 |
| Product Number: | 003 |
| Approval Date: | Jan 17, 2002 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | |
| Patent and Exclusivity Info for this product: | View |
|
|
|
| Active Ingredient: | HYDROCHLOROTHIAZIDE; VALSARTAN |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | DIOVAN HCT |
| Applicant: | NOVARTIS |
| Strength: | 12.5MG;320MG |
| Application Number: | N020818 |
| Product Number: | 004 |
| Approval Date: | Apr 28, 2006 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | |
| Patent and Exclusivity Info for this product: | View |
|
|
|
| Active Ingredient: | HYDROCHLOROTHIAZIDE; VALSARTAN |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | DIOVAN HCT |
| Applicant: | NOVARTIS |
| Strength: | 25MG;320MG |
| Application Number: | N020818 |
| Product Number: | 005 |
| Approval Date: | Apr 28, 2006 |
| Reference Listed Drug | Yes |
| RX/OTC/DISCN: | RX |
| TE Code: | |
| Patent and Exclusivity Info for this product: | View |
|
|
|
Return to Electronic Orange Book Home Page
| FDA/Center for Drug Evaluation and Research |
| Office of Generic Drugs |
| Division of Labeling and Program Support |
| Update Frequency: |
| Orange Book Data - Monthly |
| Generic Drug Product Information & Patent Information - Daily |
| Orange Book Data Updated Through December, 2009 |
| Patent and Generic Drug Product Data Last Updated: February 04, 2010 |
-
-
-