DAUNORUBICIN HYDROCHLORIDE Detail

Drug Name(s):
DAUNORUBICIN HYDROCHLORIDE

FDA Application No.:
NDA 065034

Active Ingredient(s):
DAUNORUBICIN HYDROCHLORIDE

Company:
ABRAXIS PHARM

Original Approval or Tentative Approval Date:
June 17, 2002

Products on Application NDA 065034:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
DAUNORUBICIN HYDROCHLORIDE	EQ 5MG BASE/VIAL	INJECTABLE; INJECTION	Prescription	AP

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last updated on 12-01-2008