Voretigene Neparvovec
ATC S01XA27 · 6 markets · 8 records
AU 2 records · 2 strengths
- 1 DNAunknownLUXTURNA voretigene neparvovec 5 x 10(12) (vg) per mL concentrate solution for injection vial with diluent ampoule
Records without a stated strength · 1 LUXTURNA
TW 2 records · 1 strengths
Records without a stated strength · 1 "Novartis" Luxturna concentrate and solvent for solution for injection、"諾華"樂喜達 注射劑、Luxturna concentrate and solvent for solution for injection、樂適達 注射劑
GB 1 records · 1 strengths
- 1 mLinjectionLuxturna 5 tera vector genomes/1ml concentrate and solvent for solution for injection vials
CA 1 records · 1 strengths
- 5,000,000,000,000 VGliquidLUXTURNA
ES 1 records · 1 strengths
Records without a stated strength · 1 LUXTURNA x GENOMAS VECTORIALES/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 LUXTURNA
| Strength / form / release | GB | CA | AU | ES | TW | EU |
|---|---|---|---|---|---|---|
| 1 mL injection | Luxturna 5 tera vector genomes/1ml concentrate and solvent for solution for injection vials | |||||
| 1 DNA unknown | LUXTURNA voretigene neparvovec 5 x 10(12) (vg) per mL concentrate solution for injection vial with diluent ampoule | |||||
| 5,000,000,000,000 VG check strength liquid | LUXTURNA | |||||
injection | LUXTURNA x GENOMAS VECTORIALES/ML | "Novartis" Luxturna concentrate and solvent for solution for "諾華"樂喜達 注射劑 Luxturna concentrate and solvent for solution for+1樂適達 注射劑 | ||||
unknown | LUXTURNA | LUXTURNA |
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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 and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en GB que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 GB 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 GB 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.
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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.