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Summary for Tradename: RAPAFLO
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Clinical Trials for: RAPAFLOUse of Silodosin to Treat Moderate to Severe Abacterial Chronic Prostatitis/Chronic Pelvic Pain Syndrome. Status: Completed Condition: Abacterial Chronic Prostatitis/Chronic Pelvic Pain Syndrome Effectiveness and Safety of Silodosin in the Treatment of Benign Prostatic Hyperplasia Status: Active, not recruiting Condition: Benign Prostatic Hyperplasia Safety and Efficacy of QD Versus BID Silodosin With Lower Urinary Tract Symptoms Suggestive of BPH Status: Completed Condition: Benign Prostatic Hypertrophy Study of a α1A Adrenoceptor Selective Antagonist Silodosin to Treat Severe Benign Prostatic Hyperplasia(BPH) Status: Completed Condition: Benign Prostatic Hyperplasia A Study of Silodosin 8 mg Daily for the Treatment of Nocturia in Men With Benign Prostatic Hyperplasia Status: Completed Condition: Nocturia; Prostatic Hyperplasia A Dose-finding Study of Silodosin in Patients With Urinary Calculi Status: Recruiting Condition: Urinary Calculus Efficacy and Safety of Silodosin on Voiding Dysfunction Associated With Neurogenic Bladder Status: Completed Condition: Neurogenic Bladder; Voiding Dysfunction Evaluation of the Efficacy and Safety of Silodosin in the Treatment of the Signs and Symptoms of BPH Status: Completed Condition: Benign Prostatic Hyperplasia Differential Effect of Silodosin Versus Tamsulosin on Stone Clearance After Extra-corporeal Shock Wave Lithotripsy Status: Not yet recruiting Condition: Kidney Stones Efficacy and Safety of Silodosin in the Treatment of Natural Expulsion in Patients With Ureteral Stones Status: Enrolling by invitation Condition: Ureteral Stone 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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Watson Labs | RAPAFLO | silodosin | CAPSULE; ORAL | 022206 | Oct 8, 2008 | RX | No | <disabled> | <disabled> | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Watson Labs | RAPAFLO | silodosin | CAPSULE; ORAL | 022206 | Oct 8, 2008 | RX | No | 5,387,603 | Y | Y | <disabled> | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Watson Labs | RAPAFLO | silodosin | CAPSULE; ORAL | 022206 | Oct 8, 2008 | RX | No | 5,403,847 | <disabled> | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Watson Labs | RAPAFLO | silodosin | CAPSULE; ORAL | 022206 | Oct 8, 2008 | RX | No | 5,780,485 | <disabled> | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Drugname | Dosage | Strength | RLD | Submissiondate |
| silodosin | Capsules | 4 mg and 8 mg | Rapaflo | 10/9/2012 |
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