Application 076380

Related Records

Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	JUNEL 1/20	ETHINYL ESTRADIOL; NORETHINDRONE ACETATE	TABLET;ORAL-21	0.02MG;1MG	No	No

NDC	Name	Nonproprietary name	Labeler	Marketing category	Status
0555-9025	Junel	Norethindrone Acetate and Ethinyl Estradiol	Teva Pharmaceuticals USA, Inc.	ANDA	Current
0555-9025	Junel	Norethindrone Acetate and Ethinyl Estradiol	Teva Pharmaceuticals USA, Inc.	ANDA	Current
0555-9025	Junel	Norethindrone Acetate and Ethinyl Estradiol	Teva Pharmaceuticals USA, Inc.	ANDA	Current
0555-9025	Junel	Norethindrone Acetate and Ethinyl Estradiol	Teva Pharmaceuticals USA, Inc.	ANDA	Current
0555-9025	Junel	Norethindrone Acetate and Ethinyl Estradiol	Teva Pharmaceuticals USA, Inc.	ANDA	Current
0555-9025	Junel	Norethindrone Acetate and Ethinyl Estradiol	Teva Pharmaceuticals USA, Inc.	ANDA	Current
51285-131	Loestrin	Norethindrone Acetate and Ethinyl Estradiol	Teva Women's Health, Inc.	ANDA	Current
51285-131	Loestrin	Norethindrone Acetate and Ethinyl Estradiol	Teva Women's Health, Inc.	ANDA	Current
51285-131	Loestrin	Norethindrone Acetate and Ethinyl Estradiol	Teva Women's Health, Inc.	ANDA	Current
51285-131	Loestrin	Norethindrone Acetate and Ethinyl Estradiol	Teva Women's Health, Inc.	ANDA	Current
51285-131	Loestrin	Norethindrone Acetate and Ethinyl Estradiol	Teva Women's Health, Inc.	ANDA	Current
72189-215	Junel FE	Junel FE	Direct_Rx	ANDA	Current