NDC Labeler Alexion Pharmaceuticals, Inc.

Alexion Pharmaceuticals, Inc. labeler's code is 25682. The labeler has 14 products that have an assigned National Drug Code.

NDC	Proprietary Name	Non-Proprietary Name	Dosage Form	Route Name	Product Type	Status
25682-001	Soliris	Eculizumab	Injection, Solution, Concentrate	Intravenous	Human Prescription Drug	ACTIVE
25682-007	Kanuma	Sebelipase Alfa	Injection, Solution, Concentrate	Intravenous	Human Prescription Drug	ACTIVE
25682-010	Strensiq	Asfotase Alfa	Solution	Subcutaneous	Human Prescription Drug	ACTIVE
25682-013	Strensiq	Asfotase Alfa	Solution	Subcutaneous	Human Prescription Drug	ACTIVE
25682-016	Strensiq	Asfotase Alfa	Solution	Subcutaneous	Human Prescription Drug	ACTIVE
25682-019	Strensiq	Asfotase Alfa	Solution	Subcutaneous	Human Prescription Drug	ACTIVE
25682-022	Ultomiris	Ravulizumab	Solution, Concentrate	Intravenous	Human Prescription Drug	ACTIVE
25682-025	Ultomiris	Ravulizumab	Solution, Concentrate	Intravenous	Human Prescription Drug	ACTIVE
25682-028	Ultomiris	Ravulizumab	Solution, Concentrate	Intravenous	Human Prescription Drug	ACTIVE
25682-031	Ultomiris	Ravulizumab	Kit		Human Prescription Drug	ACTIVE
25682-043	Voydeya	Danicopan	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
25682-046	Voydeya	Danicopan	Kit		Human Prescription Drug	ACTIVE
25682-049	Voydeya	Danicopan	Kit		Human Prescription Drug	ACTIVE
69853-0102	Andexxa	Andexanet Alfa	Injection, Powder, Lyophilized, For Solution	Intravenous	Human Prescription Drug	ACTIVE