NEBUPENT Detail

Drug Name(s):
NEBUPENT

FDA Application No.:
NDA 019887

Active Ingredient(s):
PENTAMIDINE ISETHIONATE

Company:
ABRAXIS PHARM

Original Approval or Tentative Approval Date:
June 14, 1989

Products on Application NDA 019887:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
PENTAMIDINE ISETHIONATE	600MG/VIAL	FOR SOLUTION; INHALATION	Prescription	none

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last updated on 11-21-2008

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