FENTANYL CITRATE Detail

Drug Name(s):
FENTANYL CITRATE

FDA Application No.:
NDA 019115

Active Ingredient(s):
FENTANYL CITRATE

Company:
HOSPIRA

Original Approval or Tentative Approval Date:
January 11, 1985

Products on Application NDA 019115:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FENTANYL CITRATE	EQ 0.05MG BASE/ML	INJECTABLE; INJECTION	Prescription	AP

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last updated on 11-21-2008

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