Tafamidis
ATC N07XX08 · 10 markets · 29 records
AU 6 records · 3 strengths
- 61 mgcapsuleCIPLA TAFAMIDIS tafamidis 61 mg soft capsule blister packTAFAMICIP tafamidis 61 mg soft capsule blister pack、Vyndamax、VYNDAMAX tafamidis 61 mg soft gelatin capsule blister pack
- 20 mgcapsuleVYNDAQEL tafamidis meglumine 20 mg soft gelatin capsule blister pack
Records without a stated strength · 1 Vyndamax
US 2 records · 2 strengths
GB 2 records · 2 strengths
CA 2 records · 2 strengths
ES 2 records · 2 strengths
HK 2 records · 1 strengths
Records without a stated strength · 1 Vyndamax、Vyndaqel
EU 2 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 TAFAMIDIS ACCORD、Vyndaqel
SG 1 records · 1 strengths
- 61 mgcapsuleVYNDAMAX SOFT GELATIN CAPSULE 61MG
CN 1 records · 1 strengths
- 61 mgcapsule维万心氯苯唑酸
TW 1 records · 1 strengths
- 61 mgcapsuleVyndamax soft Capsules 61 mg維萬心軟膠囊61毫克
| Strength / form / release | US | GB | CA | AU | SG | CN | ES | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|---|
| 61 mg capsule | Vyndamax | Vyndaqel | Vyndamax | CIPLA TAFAMIDIS tafamidis 61 mg soft capsule blister pack TAFAMICIP tafamidis 61 mg soft capsule blister pack Vyndamax+1VYNDAMAX tafamidis 61 mg soft gelatin capsule blister pack | VYNDAMAX SOFT GELATIN CAPSULE 61MG | 维万心氯苯唑酸 | Vyndaqel | Vyndamax soft Capsules 61 mg 維萬心軟膠囊61毫克 | ||
| 20 mg capsule | Vyndaqel | Vyndaqel | Vyndaqel | VYNDAQEL tafamidis meglumine 20 mg soft gelatin capsule blister pack | ||||||
| 12.2 mg capsule | Vyndaqel | |||||||||
unknown | Vyndamax | Vyndamax Vyndaqel | TAFAMIDIS ACCORD Vyndaqel |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in ES and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en ES que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 ES 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 ES 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.