LEUCOVORIN CALCIUM Detail

Drug Name(s):
LEUCOVORIN CALCIUM

FDA Application No.:
NDA 074544

Active Ingredient(s):
LEUCOVORIN CALCIUM

Company:
PAR PHARM

Original Approval or Tentative Approval Date:
August 27, 1997

Products on Application NDA 074544:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LEUCOVORIN CALCIUM	EQ 5MG BASE	TABLET; ORAL	Prescription	AB

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last updated on 12-01-2008