VANCERIL Detail

Drug Name(s):
VANCERIL

FDA Application No.:
NDA 017573

Active Ingredient(s):
BECLOMETHASONE DIPROPIONATE

Company:
SCHERING

Original Approval or Tentative Approval Date:
May 11, 1976

Products on Application NDA 017573:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
BECLOMETHASONE DIPROPIONATE	0.042MG/INH	AEROSOL, METERED; INHALATION	Discontinued	none

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last updated on 11-21-2008

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