LEUCOVORIN CALCIUM Detail

Drug Name(s):
LEUCOVORIN CALCIUM

FDA Application No.:
NDA 008107

Active Ingredient(s):
LEUCOVORIN CALCIUM

Company:
MAYNE PHARMA USA

Original Approval or Tentative Approval Date:
August 14, 1977

Products on Application NDA 008107:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LEUCOVORIN CALCIUM	EQ 60MG BASE/VIAL	FOR SOLUTION; ORAL	Discontinued	none
LEUCOVORIN CALCIUM	EQ 350MG BASE/VIAL	INJECTABLE; INJECTION	Prescription	AP
LEUCOVORIN CALCIUM	EQ 3MG BASE/ML	INJECTABLE; INJECTION	Discontinued	none

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last updated on 11-21-2008

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