Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 020885
Company: APOTEX

• Other Important Information from FDA

Products on NDA 20885

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
PAXIL	PAROXETINE HYDROCHLORIDE	EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	CAPSULE;ORAL	Discontinued	None	Yes	No
PAXIL	PAROXETINE HYDROCHLORIDE	EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	CAPSULE;ORAL	Discontinued	None	Yes	No
PAXIL	PAROXETINE HYDROCHLORIDE	EQ 30MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	CAPSULE;ORAL	Discontinued	None	Yes	No
PAXIL	PAROXETINE HYDROCHLORIDE	EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	CAPSULE;ORAL	Discontinued	None	Yes	No