VALPROIC ACID Detail

Drug Name(s):
VALPROIC ACID

FDA Application No.:
NDA 070631

Active Ingredient(s):
VALPROIC ACID

Company:
USL PHARMA

Original Approval or Tentative Approval Date:
October 5, 1989

Products on Application NDA 070631:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
VALPROIC ACID	250MG	CAPSULE; ORAL	Prescription	AB

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last updated on 12-01-2008

VALPROIC ACID Detail

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