CARBIDOPA AND LEVODOPA Detail

Drug Name(s):
CARBIDOPA AND LEVODOPA

FDA Application No.:
NDA 073587

Active Ingredient(s):
CARBIDOPA; LEVODOPA

Company:
SANDOZ

Original Approval or Tentative Approval Date:
January 7, 1997

Products on Application NDA 073587:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CARBIDOPA; LEVODOPA	25MG;100MG	TABLET; ORAL	Prescription	AB

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January 2009

CARBIDOPA AND LEVODOPA Detail

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