SUN PHARM Application 090853

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	IBANDRONATE SODIUM	IBANDRONATE SODIUM	INJECTABLE;INTRAVENOUS	EQ 3MG BASE/3ML	No	No

NDC, Name, Nonproprietary name table
NDC	Name	Nonproprietary name	Labeler	Marketing category	Status
62756-218	IBANDRONATE SODIUM	IBANDRONATE SODIUM	Sun Pharmaceutical Industries, Inc.	ANDA	Current

Document, Submission type, Date table
Document	Submission type	Date
18541	ORIG	2014-02-27
9300	ORIG	2014-02-19