PARCOPA Detail

Drug Name(s):
PARCOPA

FDA Application No.:
NDA 076699

Active Ingredient(s):
CARBIDOPA; LEVODOPA

Company:
SCHWARZ PHARMA

Original Approval or Tentative Approval Date:
August 26, 2004

Products on Application NDA 076699:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CARBIDOPA; LEVODOPA	10MG;100MG	TABLET, ORALLY DISINTEGRATING; ORAL	Prescription	none
CARBIDOPA; LEVODOPA	25MG;250MG	TABLET, ORALLY DISINTEGRATING; ORAL	Prescription	none

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last updated on 12-05-2008