LEUCOVORIN CALCIUM Detail

Drug Name(s):
LEUCOVORIN CALCIUM

FDA Application No.:
NDA 089628

Active Ingredient(s):
LEUCOVORIN CALCIUM

Company:
PHARMACHEMIE USA

Original Approval or Tentative Approval Date:
September 14, 1998

Products on Application NDA 089628:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LEUCOVORIN CALCIUM	EQ 50MG BASE/VIAL	INJECTABLE; INJECTION	Prescription	AP

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last updated on 11-21-2008

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