LEUCOVORIN CALCIUM Detail

Drug Name(s):
LEUCOVORIN CALCIUM

FDA Application No.:
NDA 075327

Active Ingredient(s):
LEUCOVORIN CALCIUM

Company:
SANDOZ

Original Approval or Tentative Approval Date:
March 23, 1999

Products on Application NDA 075327:

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 11-19-2008

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