Search results from the "OB_Rx" table for query
on "020031."
| Active Ingredient: | PAROXETINE HYDROCHLORIDE |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | PAXIL |
| Applicant: | GLAXOSMITHKLINE |
| Strength: | EQ 10MG BASE |
| Application Number: | 020031 |
| Product Number: | 001 |
| Approval Date: | Dec 29, 1992 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | AB |
| Patent and Exclusivity Info for this product: | View |
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| Active Ingredient: | PAROXETINE HYDROCHLORIDE |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | PAXIL |
| Applicant: | GLAXOSMITHKLINE |
| Strength: | EQ 20MG BASE |
| Application Number: | 020031 |
| Product Number: | 002 |
| Approval Date: | Dec 29, 1992 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | AB |
| Patent and Exclusivity Info for this product: | View |
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|
| Active Ingredient: | PAROXETINE HYDROCHLORIDE |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | PAXIL |
| Applicant: | GLAXOSMITHKLINE |
| Strength: | EQ 30MG BASE |
| Application Number: | 020031 |
| Product Number: | 003 |
| Approval Date: | Dec 29, 1992 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | AB |
| Patent and Exclusivity Info for this product: | View |
|
|
|
| Active Ingredient: | PAROXETINE HYDROCHLORIDE |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | PAXIL |
| Applicant: | GLAXOSMITHKLINE |
| Strength: | EQ 40MG BASE |
| Application Number: | 020031 |
| Product Number: | 005 |
| Approval Date: | Dec 29, 1992 |
| Reference Listed Drug | Yes |
| RX/OTC/DISCN: | RX |
| TE Code: | AB |
| Patent and Exclusivity Info for this product: | View |
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| Update Frequency: |
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| 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 |