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Filtering by: Collection FDA Drug Approval Documents

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1. Ziprasidone statistical review

Creator:: United States. Food and Drug Administration.
Date:: 2/5/2001 0:00
Document Type:: article

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2. Ziprasidone medical review

Creator:: United States. Food and Drug Administration.
Date:: 2/5/2001 0:00
Document Type:: article

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3. Venlafaxine XR

Creator:: United States. Food and Drug Administration.
Date:: 10/20/1997 0:00
Document Type:: article

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4. Venlafaxine hydrochloride XR

Creator:: United States. Food and Drug Administration.
Date:: 1/1/2003 0:00
Document Type:: article

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5. Venlafaxine hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 1/1/2005 0:00
Document Type:: article

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6. Venlafaxine hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 1918
Document Type:: article

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7. Venlafaxine

Creator:: United States. Food and Drug Administration.
Date:: 12/28/1993 0:00
Document Type:: article

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8. Sertraline hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 1/1/1999 0:00
Document Type:: article

9. Sertraline hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 1/1/2003 0:00
Document Type:: article

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10. Sertraline hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 1/1/1997 0:00
Document Type:: article

11. Sertraline hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 1/1/1996 0:00
Document Type:: article

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12. Sertraline

Creator:: United States. Food and Drug Administration.
Date:: 12/30/1991 0:00
Document Type:: article

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13. Risperidone immediate release complete Drug Approval Package (all reviews)

Creator:: United States. Food and Drug Administration.
Date:: 12/29/1993 0:00
Document Type:: article

14. Risperidone Consta complete Drug Approval Package (all reviews)

Creator:: United States. Food and Drug Administration.
Date:: 10/29/2003 0:00
Document Type:: article

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15. Quetiapine statistical review

Creator:: United States. Food and Drug Administration.
Date:: 9/26/1997 0:00
Document Type:: article

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16. Paroxetine hydrochloride CR

Creator:: United States. Food and Drug Administration.
Date:: 1/1/2003 0:00
Document Type:: article

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17. Paroxetine hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 1/1/1999 0:00
Document Type:: article

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18. Paroxetine hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 1/1/2001 0:00
Document Type:: article

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19. Paroxetine hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 1/1/1999 0:00
Document Type:: article

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20. Paroxetine hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 1/1/1996 0:00
Document Type:: article

21. Paroxetine hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 1/1/2001 0:00
Document Type:: article

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22. Paroxetine

Creator:: United States. Food and Drug Administration.
Date:: 12/29/1992 0:00
Document Type:: article

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23. Paliperidone statistical review

Creator:: United States. Food and Drug Administration.
Date:: 12/19/2006 0:00
Document Type:: article

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24. Paliperidone medical review

Creator:: United States. Food and Drug Administration.
Date:: 12/19/2006 0:00
Document Type:: article

25. Olanzapine complete Drug Approval Package (all reviews)

Creator:: United States. Food and Drug Administration.
Date:: 9/30/1996 0:00
Document Type:: article

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26. Nefazodone

Creator:: United States. Food and Drug Administration.
Date:: 12/22/1994 0:00
Document Type:: article

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27. Iloperidone summary review (Division Director)

Creator:: United States. Food and Drug Administration.
Date:: 5/6/2009 0:00
Document Type:: article

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28. Iloperidone statistical review

Creator:: United States. Food and Drug Administration.
Date:: 5/6/2009 0:00
Document Type:: article

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29. Iloperidone Office Director memo

Creator:: United States. Food and Drug Administration.
Date:: 5/6/2009 0:00
Document Type:: article

30. Iloperidone not approvable letter

Creator:: United States. Food and Drug Administration.
Date:: 5/6/2009 0:00
Document Type:: article

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31. Iloperidone medical review

Creator:: United States. Food and Drug Administration.
Date:: 5/6/2009 0:00
Document Type:: article

32. Iloperidone approval letter

Creator:: United States. Food and Drug Administration.
Date:: 5/6/2009 0:00
Document Type:: article

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33. Iloperidone adminstrative correspondence

Creator:: United States. Food and Drug Administration.
Date:: 5/6/2009 0:00
Document Type:: article

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34. Fluvoxamine maleate

Creator:: United States. Food and Drug Administration.
Date:: 1/1/2008 0:00
Document Type:: article

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35. Fluvoxamine maleate

Creator:: United States. Food and Drug Administration.
Date:: 1/1/1994 0:00
Document Type:: article

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36. Fluoxetine hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 1/1/2002 0:00
Document Type:: article

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37. Fluoxetine hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 1/1/1994 0:00
Document Type:: article

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38. Fluoxetine

Creator:: United States. Food and Drug Administration.
Date:: 12/29/1987 0:00
Document Type:: article

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39. Escitalopram oxalate

Creator:: United States. Food and Drug Administration.
Date:: 12/1/2003 0:00
Document Type:: article

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40. Duloxetine hydrochloride

Creator:: United States. Food and Drug Administration.
Date:: 2/1/2007 0:00
Document Type:: article

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41. Bupropion SR

Creator:: United States. Food and Drug Administration.
Date:: 10/4/1996 0:00
Document Type:: article

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42. Aripiprazole statistical review

Creator:: United States. Food and Drug Administration.
Date:: 11/25/2002 0:00
Document Type:: article

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43. Aripiprazole medical review

Creator:: United States. Food and Drug Administration.
Date:: 5/1/2014 0:00
Document Type:: article