PACLITAXEL Detail

Drug Name(s):
PACLITAXEL

FDA Application No.:
NDA 076233

Active Ingredient(s):
PACLITAXEL

Company:
MAYNE PHARMA USA

Original Approval or Tentative Approval Date:
July 31, 2002

Products on Application NDA 076233:

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

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last updated on 12-05-2008

PACLITAXEL Detail

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