LEVITRA Detail

FDA Consumer Information Sheet:

Patient Information Sheet

Drug Name(s):
LEVITRA

FDA Application No.:
NDA 021400

Active Ingredient(s):
VARDENAFIL HYDROCHLORIDE

Company:
BAYER PHARMS

Original Approval or Tentative Approval Date:
August 18, 2003

Products on Application NDA 021400:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
VARDENAFIL HYDROCHLORIDE	2.5MG	TABLET; ORAL	Prescription	none
VARDENAFIL HYDROCHLORIDE	5MG	TABLET; ORAL	Prescription	none

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last updated on 11-21-2008

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