Galsulfase
ATC A16AB08 · 7 markets · 8 records
AU 2 records · 2 strengths
- 5 mginjectionNAGLAZYME galsulfase-rch 5mg/5mL concentrated solution for injection vial
Records without a stated strength · 1 NAGLAZYME
US 1 records · 1 strengths
- 5 mg/5 mLliquidNAGLAZYME
GB 1 records · 1 strengths
- 5 mg/5 mLinjectionNaglazyme 5mg/5ml solution for infusion vials
CA 1 records · 1 strengths
- 1 mgliquidNAGLAZYME
SG 1 records · 1 strengths
- 5 mg/5 mLinjectionNAGLAZYME CONCENTRATE FOR SOLUTION FOR INFUSION 5MG/5ML
HK 1 records · 1 strengths
Records without a stated strength · 1 NAGLAZYME CONC SOLN FOR IV INFUSION 1MG/ML
EU 1 records · 1 strengths
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
Records without a stated strength · 1 NAGLAZYME
| Strength / form / release | US | GB | CA | AU | SG | HK | EU |
|---|---|---|---|---|---|---|---|
| 5 mg/5 mL injection | Naglazyme 5mg/5ml solution for infusion vials | NAGLAZYME CONCENTRATE FOR SOLUTION FOR INFUSION 5MG/5ML | |||||
| 5 mg/5 mL liquid | NAGLAZYME | ||||||
| 1 mg liquid | NAGLAZYME | ||||||
| 5 mg injection | NAGLAZYME galsulfase-rch 5mg/5mL concentrated solution for injection vial | ||||||
unknown | NAGLAZYME | NAGLAZYME CONC SOLN FOR IV INFUSION 1MG/ML | NAGLAZYME |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in GB · SG and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en GB · SG que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 GB · SG 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 GB · SG 有記錄(未在本表顯示)。
“not disclosed” means the source does not publish the strength — it does not mean the product has none.
Hong Kong records are name/ingredient-level only: no strength, dosage form or registration status; on the register does not prove current supply.
Australia ARTG data has no registration-status column, so status is shown as unknown; being on the register does not mean currently marketed.
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.