Tedizolid
Records for this ingredient, by country (identity only).
ATC J01XX11 · 10 markets · 17 records
GB 2 records · 2 shown of 2
- 200 mgtabletSIVEXTRO
- 200 mg per mL / per unit basis not statedinjectionSivextro 200mg powder for concentrate for solution for infusion vials
SG 2 records · 2 shown of 2
- 200 mgtabletSIVEXTRO
- 200 mg per mL / per unit basis not statedinjectionSIVEXTRO LYOPHILIZED POWDER FOR SOLUTION FOR INFUSION 200MG PER VIAL
ES 2 records · 2 shown of 2
JP 2 records · 2 shown of 2
- 200 mgtabletシベクトロ錠200mg
- 200 mg per mL / per unit basis not statedinjectionシベクトロ点滴静注用200mg
TW 1 records · 1 shown of 1
- 200 mg per mL / per unit basis not statedinjectionTedizo Lyo Injection 200MG泰帝卓凍晶注射劑200毫克
EU 1 records · 0 shown of 0
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.
1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
FR 1 records · 1 shown of 1
- 200 mgtabletSIVEXTRO 200 mg, comprimé pelliculé
Some strengths are recorded without a per mL / per unit basis. They are shown as recorded and are not compared with other markets.
| Strength / form / release | US | GB | SG | ES | TW | JP | EU | FR |
|---|---|---|---|---|---|---|---|---|
| 200 mg tablet | SIVEXTRO | SIVEXTRO | SIVEXTRO | SIVEXTRO | シベクトロ錠200mg | SIVEXTRO 200 mg, comprimé pelliculé | ||
| 200 mg per mL / per unit basis not stated cannot compare injection | Sivextro 200mg powder for concentrate for solution for infusion vials | SIVEXTRO LYOPHILIZED POWDER FOR SOLUTION FOR INFUSION 200MG PER VIAL | SIVEXTRO | Tedizo Lyo Injection 200MG 泰帝卓凍晶注射劑200毫克 | シベクトロ点滴静注用200mg | |||
| 200 mg/4 mL injection | SIVEXTRO | |||||||
unknown | SIVEXTRO |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in EU and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en EU que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 EU 有记录（未在本表显示）。 另有 1 個規格/劑型僅在 EU 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.
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.