VALPROATE SODIUM Detail

Drug Name(s):
VALPROATE SODIUM

FDA Application No.:
NDA 076295

Active Ingredient(s):
VALPROATE SODIUM

Company:
BEDFORD

Original Approval or Tentative Approval Date:
November 13, 2002

Products on Application NDA 076295:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
VALPROATE SODIUM	EQ 100MG BASE/ML	INJECTABLE; INJECTION	Prescription	AP

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January 2009

VALPROATE SODIUM Detail

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