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Exdensur — Description, Dosage, Side Effects | PillsCard
OTC
Exdensur
100 mg, Roztwór do wstrzykiwań we wstrzykiwaczu
INN: Depemokimab
Data updated: 2026-04-08
Available in:
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Form
Roztwór do wstrzykiwań we wstrzykiwaczu
Dosage
100 mg
Route
—
Storage
—
About This Product
User Reviews
Reviews reflect personal experiences and are not medical advice. Always consult your doctor.
Manufacturer
GlaxoSmithKline Trading Services Limited
ATC Code
R03DX
Source
URPL
11 DESCRIPTION Depemokimab‑ulaa is an interleukin‑5 (IL‑5) antagonist monoclonal antibody (humanized Immunoglobulin G1 [IgG1] kappa). Depemokimab‑ulaa is produced by recombinant DNA technology in Chinese hamster ovary cells. The estimated molecular weight of depemokimab‑ulaa is 149 kDa. EXDENSUR (depemokimab‑ulaa) injection is a sterile, preservative‑free, colorless, yellow to brown, clear to opalescent solution for subcutaneous (SC) use. EXDENSUR injection is supplied in a single‑dose, 1‑mL, prefilled pen with a fixed 29‑gauge, half‑inch needle or in a single‑dose, 1‑mL, prefilled syringe with a fixed 29‑gauge, half‑inch needle with a needle guard. Each 1 mL delivers 100 mg depemokimab‑ulaa, (8.43 mg) arginine HCl, (0.017 mg) edetate disodium, (1.41 mg) histidine, (2.29 mg) L‑histidine HCl monohydrate, (0.20 mg) polysorbate 80, (61.6 mg) trehalose, and Water for Injection with a pH of 6.0.
⚠️ Warnings
For single-use only.
Do not shake
Before administration, the solution must be inspected visually. The liquid must be colourless, yellow to brown, clear to opalescent. If the solution is cloudy, discoloured or contains particles, the solution must not be used.
After removing the pre-filled pen from the refrigerator, allow the pen to reach room temperature for at least 30 minutes before injecting EXDENSUR.
Comprehensive instructions for subcutaneous administration of EXDENSUR in a pre-filled pen are provided at the end of the package leaflet.
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.