VALPROIC ACID Detail

Drug Name(s):
VALPROIC ACID

FDA Application No.:
NDA 073178

Active Ingredient(s):
VALPROIC ACID

Company:
TEVA PHARMS

Original Approval or Tentative Approval Date:
August 24, 1992

Products on Application NDA 073178:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
VALPROIC ACID	250MG/5ML	SYRUP; ORAL	Prescription	AA

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last updated on 12-01-2008

VALPROIC ACID Detail

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