Ritlecitinib
ATC L04AF08 · 11 markets · 14 records
AU 3 records · 2 strengths
- 80.128 mgcapsuleLITFULO ritlecitinib (as tosylate) 50 mg hard capsule blister packLITFULO ritlecitinib (as tosylate) 50 mg hard capsule bottle
Records without a stated strength · 1 Litfulo
US 2 records · 1 strengths
- 50 mgcapsuleLitfulo
GB 1 records · 1 strengths
- 50 mgcapsuleLitfulo
CA 1 records · 1 strengths
- 50 mgcapsuleLitfulo
SG 1 records · 1 strengths
- 50 mgcapsuleLitfulo
CN 1 records · 1 strengths
- 50 mgcapsule乐复诺甲苯磺酸利特昔替尼
ES 1 records · 1 strengths
- 50 mgcapsuleLitfulo
MX 1 records · 1 strengths
Records without a stated strength · 1 Litfulo
TW 1 records · 1 strengths
- 50 mgcapsuleLitfulo立服樂50毫克膠囊
HK 1 records · 1 strengths
Records without a stated strength · 1 Litfulo
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 Litfulo
| Strength / form / release | US | GB | CA | AU | SG | CN | ES | MX | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 50 mg capsule | Litfulo | Litfulo | Litfulo | Litfulo | 乐复诺甲苯磺酸利特昔替尼 | Litfulo | Litfulo 立服樂50毫克膠囊 | ||||
| 80.128 mg capsule | LITFULO ritlecitinib (as tosylate) 50 mg hard capsule blister pack LITFULO ritlecitinib (as tosylate) 50 mg hard capsule bottle | ||||||||||
unknown | Litfulo | Litfulo | Litfulo | ||||||||
capsule | Litfulo |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in MX and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en MX que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 MX 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 MX 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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.