NAFCILLIN SODIUM Detail

Drug Name(s):
NAFCILLIN SODIUM

FDA Application No.:
NDA 062732

Active Ingredient(s):
NAFCILLIN SODIUM

Company:
SANDOZ

Original Approval or Tentative Approval Date:
December 22, 1986

Products on Application NDA 062732:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NAFCILLIN SODIUM	EQ 1GM BASE/VIAL	INJECTABLE; INJECTION	Prescription	AP

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last updated on 12-01-2008