MAPROTILINE HYDROCHLORIDE Detail

Drug Name(s):
MAPROTILINE HYDROCHLORIDE

FDA Application No.:
NDA 071944

Active Ingredient(s):
MAPROTILINE HYDROCHLORIDE

Company:
WATSON LABS

Products on Application NDA 071944:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
MAPROTILINE HYDROCHLORIDE	50MG	TABLET; ORAL	Discontinued	none

Recall Notices

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January 2009

MAPROTILINE HYDROCHLORIDE Detail

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