NDC Labeler Sumitomo Pharma America, Inc.

Sumitomo Pharma America, Inc. labeler's code is 63402. The labeler has 18 products that have an assigned National Drug Code.

NDC	Proprietary Name	Non-Proprietary Name	Dosage Form	Route Name	Product Type	Status
63402-190	Lunesta	Eszopiclone	Tablet, Coated	Oral	Human Prescription Drug	ACTIVE
63402-191	Lunesta	Eszopiclone	Tablet, Coated	Oral	Human Prescription Drug	ACTIVE
63402-193	Lunesta	Eszopiclone	Tablet, Coated	Oral	Human Prescription Drug	ACTIVE
63402-202	Aptiom	Eslicarbazepine Acetate	Tablet	Oral	Human Prescription Drug	ACTIVE
63402-204	Aptiom	Eslicarbazepine Acetate	Tablet	Oral	Human Prescription Drug	ACTIVE
63402-206	Aptiom	Eslicarbazepine Acetate	Tablet	Oral	Human Prescription Drug	ACTIVE
63402-208	Aptiom	Eslicarbazepine Acetate	Tablet	Oral	Human Prescription Drug	ACTIVE
63402-248	Aptiom	Eslicarbazepine Acetate	Kit	Oral	Human Prescription Drug	ACTIVE
63402-302	Latuda	Lurasidone Hydrochloride	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
63402-304	Latuda	Lurasidone Hydrochloride	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
63402-306	Latuda	Lurasidone Hydrochloride	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
63402-308	Latuda	Lurasidone Hydrochloride	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
63402-312	Latuda	Lurasidone Hydrochloride	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
72359-001	Rethymic	Allogenic Thymocyte-depleted Thymus Tissue-agdc	Implant	Intramuscular	Human Prescription Drug	ACTIVE
72974-120	Orgovyx	Relugolix	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
72974-415	Myfembree	Relugolix, Estradiol Hemihydrate, And Norethindrone Acetate	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
72974-120		Relugolix	Tablet, Film Coated		Drug For Further Processing	UNFINISHED
73336-075	Gemtesa	Vibegron	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE