MANDOL Detail

Drug Name(s):
MANDOL

FDA Application No.:
NDA 062560

Active Ingredient(s):
CEFAMANDOLE NAFATE

Company:
LILLY

Original Approval or Tentative Approval Date:
September 9, 1985

Products on Application NDA 062560:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CEFAMANDOLE NAFATE	EQ 2GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	none

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last updated on 12-01-2008

MANDOL Detail

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