FOUGERA PHARMS Application 075373

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	BETAMETHASONE DIPROPIONATE	BETAMETHASONE DIPROPIONATE	OINTMENT, AUGMENTED;TOPICAL	EQ 0.05% BASE	No	No

NDC, Name, Nonproprietary name table
NDC	Name	Nonproprietary name	Labeler	Marketing category	Status
0168-0268	Betamethasone Dipropionate	betamethasone dipropionate	E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.	ANDA	Current
0168-0268	Betamethasone Dipropionate	betamethasone dipropionate	E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.	ANDA	Current
0168-0268	Betamethasone Dipropionate	betamethasone dipropionate	E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.	ANDA	Current

Document, Submission type, Date table
Document	Submission type	Date
22464	ORIG	2002-01-17
8638	ORIG	1999-06-22