Search results from the "OB_Rx" table for query
on "021283."
| Active Ingredient: | VALSARTAN |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | DIOVAN |
| Applicant: | NOVARTIS |
| Strength: | 80MG |
| Application Number: | 021283 |
| Product Number: | 001 |
| Approval Date: | Jul 18, 2001 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | |
| Patent and Exclusivity Info for this product: | View |
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| Active Ingredient: | VALSARTAN |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | DIOVAN |
| Applicant: | NOVARTIS |
| Strength: | 160MG |
| Application Number: | 021283 |
| Product Number: | 002 |
| Approval Date: | Jul 18, 2001 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | |
| Patent and Exclusivity Info for this product: | View |
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| Active Ingredient: | VALSARTAN |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | DIOVAN |
| Applicant: | NOVARTIS |
| Strength: | 320MG |
| Application Number: | 021283 |
| Product Number: | 003 |
| Approval Date: | Jul 18, 2001 |
| Reference Listed Drug | Yes |
| RX/OTC/DISCN: | RX |
| TE Code: | |
| Patent and Exclusivity Info for this product: | View |
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| Active Ingredient: | VALSARTAN |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | DIOVAN |
| Applicant: | NOVARTIS |
| Strength: | 40MG |
| Application Number: | 021283 |
| Product Number: | 004 |
| Approval Date: | Aug 14, 2002 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | |
| Patent and Exclusivity Info for this product: | View |
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| 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 October, 2009 |
| Patent and Generic Drug Product Data Last Updated: November 20, 2009 |