LEUCOVORIN CALCIUM Detail

Drug Name(s):
LEUCOVORIN CALCIUM

FDA Application No.:
NDA 071199

Active Ingredient(s):
LEUCOVORIN CALCIUM

Company:
BARR

Original Approval or Tentative Approval Date:
February 21, 1991

Products on Application NDA 071199:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LEUCOVORIN CALCIUM	EQ 25MG BASE	TABLET; ORAL	Prescription	AB

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last updated on 12-01-2008