Home Canadian DIN search LANADELUMAB DIN 02566257
TAKHZYRO DIN 02566257
Status: Approved
Holder: TAKEDA CANADA INC
Health Canada record
Active ingredient(s) LANADELUMAB 150 MG Dosage form Solution Route Subcutaneous Schedule PRESCRIPTION; SCHEDULE D Class Human ATC B06AC05 LANADELUMAB Original market date Current status date 02-Mar-2026 Source Health Canada DPD
Establishment licence of the holder Takeda Canada Inc. — licence 101769, currently licensed, last inspection rating C (2026-02-24).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing LANADELUMAB DIN Product Company Form Strength Status 02480948 TAKHZYRO TAKEDA CANADA INC Solution LANADELUMAB 300 MG Marketed 02505614 TAKHZYRO TAKEDA CANADA INC Solution LANADELUMAB 300 MG Marketed 02564483 TAKHZYRO TAKEDA CANADA INC Solution LANADELUMAB 300 MG Marketed
Notices of Compliance NOC Date Submission Reason 37076 2026-03-02 Supplement to a New Drug Submission (SNDS) Expansion of the indication and addition of a strength:
TAKHZYRO (lanadelumab injection) is indicated for:
• routine prevention of attacks of hereditary angioedema (HAE) in adults and pediatric patients aged 2 years and older.
TAKHZYRO is not intended for acute treatment of HAE attacks
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