BENZEDRINE Detail

Drug Name(s):
BENZEDRINE

FDA Application No.:
NDA 083900

Active Ingredient(s):
AMPHETAMINE SULFATE

Company:
SMITH KLINE & FRENCH

Original Approval or Tentative Approval Date:
April 14, 1976

Products on Application NDA 083900:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
AMPHETAMINE SULFATE	10MG	Tablet; Oral	Discontinued	none

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last updated on 11-19-2008

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