DANTRIUM Detail

Drug Name(s):
DANTRIUM

FDA Application No.:
NDA 017443

Active Ingredient(s):
DANTROLENE SODIUM

Company:
PROCTER AND GAMBLE

Original Approval or Tentative Approval Date:
January 14, 1974

Products on Application NDA 017443:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
DANTROLENE SODIUM	25MG	CAPSULE; ORAL	Prescription	AB
DANTROLENE SODIUM	50MG	CAPSULE; ORAL	Prescription	AB

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last updated on 11-21-2008

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