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Summary for Tradename: PAXIL CR
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| Pharmacology for Tradename: PAXIL CR
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Clinical Trials for: PAXIL CRRepeat Dose Study of Controlled-Release Paroxetine Tablets and Immediate-Release Paroxetine Tablets in Healthy Japanese Male Subjects Status: Completed Condition: Depressive Disorder; Healthy Volunteer Paroxetine-CR (Paxil-CR) in the Treatment of Patients With Fibromyalgia Syndrome Status: Completed Condition: Fibromyalgia Syndrome Effectiveness Study of Mirtazapine Combined With Paroxetine in Major Depressive Patients Without Early Improvement Status: Recruiting Condition: Major Depression Paxil CR Bioequivalence Study Brazil - Fed Administration Status: Completed Condition: Depressive Disorder; Healthy Volunteers Paxil Japanese Post Marketing Paediatric Study in Depression (Double-blind, Placebo Controlled Study) Status: Completed Condition: Major Depressive Disorder; Depressive Disorder PAXIL CR Bioequivalence Study Status: Completed Condition: Two Single Doses of Controlled Release Paroxetine Given 14 Days Apart; Depressive Disorder; Healthy Volunteer Controlled-release Paroxetine in Major Depressive Disorder (Double-blind, Placebo-controlled Study) Status: Completed Condition: Depressive Disorder; Major Depressive Disorder (MDD) A Local Register Study For Major Depression Of Paroxetine Controlled Release Status: Completed Condition: Depressive Disorder, Major; Major Depressive Disorder (MDD) Fasting Study of Paroxetine Hydrochloride Controlled-Release Tablets 25 mg to Paxil CRâ„¢ Tablets 25 mg Status: Completed Condition: Healthy Food Study of Paroxetine Hydrochloride Controlled-Release Tablets 25 mg to Paxil CRâ„¢ Tablets 25 mg Status: Completed Condition: Healthy Courtesy of ClinicalTrials.org See more clinical trials for this drug | ||||||||||||||
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Type | RLD | Patent No. | Product | Substance | Delist_Flag | Patent Expiration | Exclusivity Expiration | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Glaxosmithkline | PAXIL CR | paroxetine hydrochloride | TABLET, EXTENDED RELEASE; ORAL | 020936 | Dec 6, 2000 | RX | Yes | 5,422,123*PED | <disabled> | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Glaxosmithkline | PAXIL CR | paroxetine hydrochloride | TABLET, EXTENDED RELEASE; ORAL | 020936 | Dec 6, 2000 | RX | Yes | 5,872,132*PED | Y | <disabled> | <disabled> | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Glaxosmithkline | PAXIL CR | paroxetine hydrochloride | TABLET, EXTENDED RELEASE; ORAL | 020936 | Dec 6, 2000 | RX | Yes | 5,900,423*PED | Y | <disabled> | <disabled> | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Glaxosmithkline | PAXIL CR | paroxetine hydrochloride | TABLET, EXTENDED RELEASE; ORAL | 020936 | Dec 6, 2000 | RX | Yes | 6,121,291*PED | Y | <disabled> | <disabled> | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Drugname | Dosage | Strength | RLD | Submissiondate |
| paroxetine hydrochloride | Extended-release Tablets | 37.5 mg | Paxil CR | 5/19/2009 |
| paroxetine hydrochloride | Extended-release Tablets | 25 mg | Paxil CR | 9/9/2005 |
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