IMIPRAMINE HYDROCHLORIDE Detail

Drug Name(s):
IMIPRAMINE HYDROCHLORIDE

FDA Application No.:
NDA 089497

Active Ingredient(s):
IMIPRAMINE HYDROCHLORIDE

Company:
PAR PHARM

Original Approval or Tentative Approval Date:
August 18, 1988

Products on Application NDA 089497:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
IMIPRAMINE HYDROCHLORIDE	25MG	TABLET; ORAL	Prescription	AB

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January 2009

IMIPRAMINE HYDROCHLORIDE Detail

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