AMOXIL Detail

Drug Name(s):
AMOXIL

FDA Application No.:
NDA 062226

Active Ingredient(s):
AMOXICILLIN

Company:
GLAXOSMITHKLINE

Original Approval or Tentative Approval Date:
November 26, 1979

Products on Application NDA 062226:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
AMOXICILLIN	125MG/5ML	FOR SUSPENSION; ORAL	Prescription	AB
AMOXICILLIN	125MG/5ML	FOR SUSPENSION; ORAL	Prescription	AB
AMOXICILLIN	50MG/ML	FOR SUSPENSION; ORAL	Prescription	AB

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last updated on 12-01-2008