SUN PHARM Application 090508

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	FINASTERIDE	FINASTERIDE	TABLET;ORAL	1MG	No	No

NDC, Name, Nonproprietary name table
NDC	Name	Nonproprietary name	Labeler	Marketing category	Status
47335-714	Finasteride	Finasteride	Sun Pharmaceutical Industries, Inc.	ANDA	Current
47335-714	Finasteride	Finasteride	Sun Pharmaceutical Industries, Inc.	ANDA	Current