MAPROTILINE HYDROCHLORIDE Detail

Drug Name(s):
MAPROTILINE HYDROCHLORIDE

FDA Application No.:
NDA 072131

Active Ingredient(s):
MAPROTILINE HYDROCHLORIDE

Company:
AM THERAP

Products on Application NDA 072131:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
MAPROTILINE HYDROCHLORIDE	75MG	TABLET; ORAL	Discontinued	none

Recall Notices

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FDA Announces Class I Recall of Ophthalmic Surgical Device
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KRC Food Trading Inc. Recall of Fish Cake Sushi (December 23)

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January 2009

MAPROTILINE HYDROCHLORIDE Detail

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