Active substance
Human immunoglobulin proteins
- SFDA 6
SFDA Saudi Arabia — SFDA human drug list
| Trade name | Strength | Form · route | Pack | Public price | Type | Company | Status |
|---|---|---|---|---|---|---|---|
| PANZYGA | 100 mg/ml | Solution for infusion · Intravenous use | 1 Vial | SAR 448.30 | Biological · Prescription | OCTAPHARMA AG | Valid |
| PANZYGA | 100 mg/ml | Solution for infusion · Intravenous use | 1 Vial | SAR 1120.70 | Biological · Prescription | OCTAPHARMA AG | Valid |
| PANZYGA | 100 mg/ml | Solution for infusion · Intravenous use | 1 Vial | SAR 2241.40 | Biological · Prescription | OCTAPHARMA AG | Valid |
| PANZYGA | 100 mg/ml | Solution for infusion · Intravenous use | 1 Vial | SAR 13448.40 | Biological · Prescription | OCTAPHARMA AG | Valid |
| PANZYGA | 100 mg/ml | Solution for infusion · Intravenous use | 1 Vial | SAR 8965.60 | Biological · Prescription | OCTAPHARMA AG | Valid |
| PANZYGA | 100 mg/ml | Solution for infusion · Intravenous use | 1 Vial | SAR 4482.80 | Biological · Prescription | OCTAPHARMA AG | Valid |
Indications — CHI Daman Drug Formulary
OPTIC NEURITIS
Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.