From PR Newswire - Aug 26, 2008
TITUSVILLE, N.J., August 26, 2008 /PRNewswire/ -- Johnson & Johnson
Pharmaceutical Research & Development, L.L.C. announced today that the
FDA has asked for additional data before it will approve the company's
NDA for paliperidone palmitate, an investigational once-monthly atypical
antipsychotic intramuscular injection for treating schizophrenia and
preventing recurrence of its symptoms.
"People Who experience mood swings, fear, voices and visions"