Drug Details: VALPROATE SODIUM

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	VALPROATE SODIUM
FDA Application No:	(ANDA) 076539
Active Ingredient(s):	VALPROATE SODIUM
Company:	ABRAXIS PHARM
Original Approval or Tentative Approval Date:	June 26, 2003

Therapeutic Equivalents	Labels are not available
Approval History, Letters, Reviews and Related Documents

You can see the products in the same application. The table can be sorted by clicking the header columns.

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
VALPROATE SODIUM	VALPROATE SODIUM	EQ 100MG BASE/ML	INJECTABLE; INJECTION	Prescription	No	AP

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