ZINECARD Detail

Drug Name(s):
ZINECARD

FDA Application No.:
NDA 020212

Active Ingredient(s):
DEXRAZOXANE HYDROCHLORIDE

Company:
PHARMACIA AND UPJOHN

Original Approval or Tentative Approval Date:
May 7, 2001

Products on Application NDA 020212:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
DEXRAZOXANE HYDROCHLORIDE	EQ 250MG BASE/VIAL	INJECTABLE; INJECTION	Prescription	AP

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last updated on 11-21-2008

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