DALMANE Detail

Drug Name(s):
DALMANE

FDA Application No.:
NDA 016721

Active Ingredient(s):
FLURAZEPAM HYDROCHLORIDE

Company:
VALEANT PHARM INTL

Original Approval or Tentative Approval Date:
April 6, 1970

Products on Application NDA 016721:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FLURAZEPAM HYDROCHLORIDE	30MG	CAPSULE; ORAL	Prescription	AB

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last updated on 11-21-2008

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