LEUCOVORIN CALCIUM Detail

Drug Name(s):
LEUCOVORIN CALCIUM

FDA Application No.:
NDA 071104

Active Ingredient(s):
LEUCOVORIN CALCIUM

Company:
XANODYNE PHARM

Original Approval or Tentative Approval Date:
March 3, 1987

Products on Application NDA 071104:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LEUCOVORIN CALCIUM	EQ 15MG BASE	TABLET; ORAL	Prescription	AB

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last updated on 12-01-2008