ELIXOPHYLLIN Detail

Drug Name(s):
ELIXOPHYLLIN

FDA Application No.:
NDA 085186

Active Ingredient(s):
THEOPHYLLINE

Company:
FOREST LABS

Original Approval or Tentative Approval Date:
March 4, 1982

Products on Application NDA 085186:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
THEOPHYLLINE	80MG/15ML	ELIXIR; ORAL	Prescription	AA

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last updated on 12-05-2008

ELIXOPHYLLIN Detail

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