CHARTWELL Application 075987

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	OXAPROZIN	OXAPROZIN	TABLET;ORAL	600MG	No	No

NDC, Name, Nonproprietary name table
NDC	Name	Nonproprietary name	Labeler	Marketing category	Status
62135-176	OXAPROZIN	OXAPROZIN	Chartwell RX, LLC.	ANDA	Current
62135-176	OXAPROZIN	OXAPROZIN	Chartwell RX, LLC.	ANDA	Current