Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 007335
Company: APOTHECON

Products on NDA 7335

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
PRONESTYL	PROCAINAMIDE HYDROCHLORIDE	250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	CAPSULE;ORAL	Discontinued	None	Yes	No
PRONESTYL	PROCAINAMIDE HYDROCHLORIDE	100MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	INJECTABLE;INJECTION	Discontinued	None	Yes	No
PRONESTYL	PROCAINAMIDE HYDROCHLORIDE	500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	CAPSULE;ORAL	Discontinued	None	Yes	No
PRONESTYL	PROCAINAMIDE HYDROCHLORIDE	375MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	CAPSULE;ORAL	Discontinued	None	Yes	No
PRONESTYL	PROCAINAMIDE HYDROCHLORIDE	500MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	INJECTABLE;INJECTION	Discontinued	None	Yes	No