Fezolinetant
ATC G02CX06 · 9 markets · 12 records
US 3 records · 1 strengths
- 45 mgtabletVEOZAH
AU 2 records · 2 strengths
- 45 mgtabletVEOZA fezolinetant 45 mg film coated tablet blister pack
Records without a stated strength · 1 Veoza 45mg tablets
GB 1 records · 1 strengths
- 45 mgtabletVeoza 45mg tablets
CA 1 records · 1 strengths
- 45 mgtabletVEOZAH
SG 1 records · 1 strengths
- 45 mgtabletVEOZA™ FILM-COATED TABLETS 45 MG
ES 1 records · 1 strengths
- 45 mgtabletVeoza 45mg tablets
MX 1 records · 1 strengths
Records without a stated strength · 1 Veoza 45mg tablets
HK 1 records · 1 strengths
Records without a stated strength · 1 Veoza 45mg tablets
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 Veoza 45mg tablets
| Strength / form / release | US | GB | CA | AU | SG | ES | MX | HK | EU |
|---|---|---|---|---|---|---|---|---|---|
| 45 mg tablet | VEOZAH | Veoza 45mg tablets | VEOZAH | VEOZA fezolinetant 45 mg film coated tablet blister pack | VEOZA™ FILM-COATED TABLETS 45 MG | Veoza 45mg tablets | |||
unknown | Veoza 45mg tablets | Veoza 45mg tablets | Veoza 45mg tablets | ||||||
tablet | Veoza 45mg tablets |
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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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.