FENTANYL CITRATE Detail

Drug Name(s):
FENTANYL CITRATE

FDA Application No.:
NDA 073488

Active Ingredient(s):
FENTANYL CITRATE

Company:
WATSON LABS

Products on Application NDA 073488:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FENTANYL CITRATE	EQ 0.05MG BASE/ML	INJECTABLE; INJECTION	Discontinued	none

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last updated on 12-01-2008

FENTANYL CITRATE Detail

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