MAPROTILINE HYDROCHLORIDE Detail

Drug Name(s):
MAPROTILINE HYDROCHLORIDE

FDA Application No.:
NDA 072163

Active Ingredient(s):
MAPROTILINE HYDROCHLORIDE

Company:
WATSON LABS

Original Approval or Tentative Approval Date:
May 31, 1988

Products on Application NDA 072163:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
MAPROTILINE HYDROCHLORIDE	50MG	TABLET; ORAL	Prescription	AB

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January 2009

MAPROTILINE HYDROCHLORIDE Detail

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