PACLITAXEL Detail

Drug Name(s):
PACLITAXEL

FDA Application No.:
NDA 076131

Active Ingredient(s):
PACLITAXEL

Company:
MAYNE PHARMA USA

Original Approval or Tentative Approval Date:
May 7, 2002

Products on Application NDA 076131:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
PACLITAXEL	6MG/ML	INJECTABLE; INJECTION	Prescription	AP

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last updated on 11-19-2008

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