Health Canada drug identification number

DIN 00839191 — SANDOSTATIN 50 MCG

SANDOSTATIN is a solution of Octreotide marketed by NOVARTIS PHARMACEUTICALS CANADA INC. The full Octreotide monograph covers indications, dosing, interactions and counselling for every strength and manufacturer.

DIN
00839191
Brand name
SANDOSTATIN
Active ingredient
Octreotide
Strength
50 MCG
Dosage form
SOLUTION
Route
INTRAVENOUS; SUBCUTANEOUS
Manufacturer
NOVARTIS PHARMACEUTICALS CANADA INC
Health Canada status
MARKETED
Drug class
Somatostatin analogue

Product data from the Health Canada Drug Product Database, synced . Verify the live status at Health Canada.

Other Octreotide products

DINBrandStrengthFormManufacturerStatus
02248640 OCTREOTIDE ACETATE OMEGA 100 MCG SOLUTION OMEGA LABORATORIES LIMITED MARKETED
02248642 OCTREOTIDE ACETATE OMEGA 200 MCG SOLUTION OMEGA LABORATORIES LIMITED MARKETED
02248639 OCTREOTIDE ACETATE OMEGA 50 MCG SOLUTION OMEGA LABORATORIES LIMITED MARKETED
02248641 OCTREOTIDE ACETATE OMEGA 500 MCG SOLUTION OMEGA LABORATORIES LIMITED MARKETED
02567776 OCTREOTIDE DEPOT 10 MG POWDER FOR SUSPENSION (SUSTAINED-RELEASE STERIMAX INC MARKETED
02567784 OCTREOTIDE DEPOT 20 MG POWDER FOR SUSPENSION (SUSTAINED-RELEASE STERIMAX INC MARKETED
02567792 OCTREOTIDE DEPOT 30 MG POWDER FOR SUSPENSION (SUSTAINED-RELEASE STERIMAX INC MARKETED
02560240 OCTREOTIDE INJECTION 100 MCG SOLUTION STERIMAX INC MARKETED
02560283 OCTREOTIDE INJECTION 200 MCG SOLUTION STERIMAX INC MARKETED
02560291 OCTREOTIDE INJECTION 500 MCG SOLUTION STERIMAX INC MARKETED
02239323 SANDOSTATIN LAR 10 MG POWDER FOR SUSPENSION (SUSTAINED-RELEASE NOVARTIS PHARMACEUTICALS CANADA INC MARKETED
02239324 SANDOSTATIN LAR 20 MG POWDER FOR SUSPENSION (SUSTAINED-RELEASE NOVARTIS PHARMACEUTICALS CANADA INC MARKETED
02239325 SANDOSTATIN LAR 30 MG POWDER FOR SUSPENSION (SUSTAINED-RELEASE NOVARTIS PHARMACEUTICALS CANADA INC MARKETED

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