LARODOPA Detail

Drug Name(s):
LARODOPA

FDA Application No.:
NDA 016912

Active Ingredient(s):
LEVODOPA

Company:
ROCHE

Original Approval or Tentative Approval Date:
June 3, 1970

Products on Application NDA 016912:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LEVODOPA	100MG	CAPSULE; ORAL	Discontinued	none
LEVODOPA	500MG	CAPSULE; ORAL	Discontinued	none
LEVODOPA	500MG	TABLET; ORAL	Discontinued	none

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last updated on 11-21-2008

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