DANTROLENE SODIUM Detail

Drug Name(s):
DANTROLENE SODIUM

FDA Application No.:
NDA 076686

Active Ingredient(s):
DANTROLENE SODIUM

Company:
ACTAVIS TOTOWA

Original Approval or Tentative Approval Date:
October 23, 2005

Products on Application NDA 076686:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
DANTROLENE SODIUM	100MG	CAPSULE; ORAL	Prescription	AB
DANTROLENE SODIUM	25MG	CAPSULE; ORAL	Prescription	AB

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last updated on 12-05-2008