BECONASE AQ Detail

Drug Name(s):
BECONASE AQ

FDA Application No.:
NDA 019389

Active Ingredient(s):
BECLOMETHASONE DIPROPIONATE MONOHYDRATE

Company:
GLAXOSMITHKLINE

Original Approval or Tentative Approval Date:
August 18, 1988

Products on Application NDA 019389:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
BECLOMETHASONE DIPROPIONATE MONOHYDRATE	EQ 0.042MG DIPROP/SPRAY	SPRAY, METERED; NASAL	Prescription	none

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last updated on 11-21-2008

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