EDEX Detail

Drug Name(s):
EDEX

FDA Application No.:
NDA 020649

Active Ingredient(s):
ALPROSTADIL

Company:
SCHWARZ PHARMA

Original Approval or Tentative Approval Date:
June 11, 1997

Products on Application NDA 020649:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
ALPROSTADIL	0.01MG/VIAL	INJECTABLE; INJECTION	Prescription	AP
ALPROSTADIL	0.02MG/VIAL	INJECTABLE; INJECTION	Prescription	none
ALPROSTADIL	0.04MG/VIAL	INJECTABLE; INJECTION	Prescription	AP

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last updated on 11-21-2008

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