Search results from the "OB_Rx" table for query
on "022047."
| Active Ingredient: | QUETIAPINE FUMARATE |
| Dosage Form;Route: | TABLET, EXTENDED RELEASE; ORAL |
| Proprietary Name: | SEROQUEL XR |
| Applicant: | ASTRAZENECA |
| Strength: | EQ 50MG BASE |
| Application Number: | 022047 |
| Product Number: | 001 |
| Approval Date: | May 17, 2007 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | |
| Patent and Exclusivity Info for this product: | View |
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| Active Ingredient: | QUETIAPINE FUMARATE |
| Dosage Form;Route: | TABLET, EXTENDED RELEASE; ORAL |
| Proprietary Name: | SEROQUEL XR |
| Applicant: | ASTRAZENECA |
| Strength: | EQ 200MG BASE |
| Application Number: | 022047 |
| Product Number: | 002 |
| Approval Date: | May 17, 2007 |
| Reference Listed Drug | Yes |
| RX/OTC/DISCN: | RX |
| TE Code: | |
| Patent and Exclusivity Info for this product: | View |
|
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|
| Active Ingredient: | QUETIAPINE FUMARATE |
| Dosage Form;Route: | TABLET, EXTENDED RELEASE; ORAL |
| Proprietary Name: | SEROQUEL XR |
| Applicant: | ASTRAZENECA |
| Strength: | EQ 300MG BASE |
| Application Number: | 022047 |
| Product Number: | 003 |
| Approval Date: | May 17, 2007 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | |
| Patent and Exclusivity Info for this product: | View |
|
|
|
| Active Ingredient: | QUETIAPINE FUMARATE |
| Dosage Form;Route: | TABLET, EXTENDED RELEASE; ORAL |
| Proprietary Name: | SEROQUEL XR |
| Applicant: | ASTRAZENECA |
| Strength: | EQ 400MG BASE |
| Application Number: | 022047 |
| Product Number: | 004 |
| Approval Date: | May 17, 2007 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | |
| Patent and Exclusivity Info for this product: | View |
|
|
|
| Active Ingredient: | QUETIAPINE FUMARATE |
| Dosage Form;Route: | TABLET, EXTENDED RELEASE; ORAL |
| Proprietary Name: | SEROQUEL XR |
| Applicant: | ASTRAZENECA |
| Strength: | EQ 150MG BASE |
| Application Number: | 022047 |
| Product Number: | 005 |
| Approval Date: | Aug 11, 2008 |
| 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 |