Doravirine
ATC J05AG06 · 11 markets · 21 records
US 4 records · 1 strengths
- 100 mgtabletDELSTRIGOIDVYNSO、PIFELTRO
CA 3 records · 1 strengths
- 100 mgtabletDELSTRIGOIDVYNSO、PIFELTRO
GB 2 records · 1 strengths
- 100 mgtabletDELSTRIGOPIFELTRO
TW 2 records · 1 strengths
Records without a stated strength · 1 DELSTRIGO、PIFELTRO、平菲妥膜衣錠、達滋克膜衣錠
HK 2 records · 1 strengths
Records without a stated strength · 1 DELSTRIGO、PIFELTRO
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 DELSTRIGO、PIFELTRO
AU 1 records · 1 strengths
- 100 mgtabletPIFELTRO doravirine 100 mg film-coated tablet bottle
SG 1 records · 1 strengths
- 100 mgtabletPIFELTRO
CN 1 records · 1 strengths
- 100 mgtablet沛卓多拉韦林
ES 1 records · 1 strengths
- 100 mgtabletPIFELTRO
| Strength / form / release | US | GB | CA | AU | SG | CN | ES | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|---|
| 100 mg tablet | DELSTRIGO IDVYNSO PIFELTRO | DELSTRIGO PIFELTRO | DELSTRIGO IDVYNSO PIFELTRO | PIFELTRO doravirine 100 mg film-coated tablet bottle | PIFELTRO | 沛卓多拉韦林 | PIFELTRO | |||
tablet | DELSTRIGO PIFELTRO 平菲妥膜衣錠+1達滋克膜衣錠 | |||||||||
unknown | DELSTRIGO PIFELTRO | DELSTRIGO PIFELTRO |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in HK · EU and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en HK · EU que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 HK · EU 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 HK · 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.
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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.