Elvitegravir
ATC J05AR09 · 8 markets · 28 records
GB 6 records · 3 strengths
- 150 mgtabletGenvoyaStribild、Vitekta 85mg tablets
- 90 mgtabletGenvoya
- 85 mgtabletVitekta 85mg tablets
AU 5 records · 2 strengths
- 150 mgtabletGenvoyaGENVOYA elvitegravir (150mg), cobicistat (150mg), emtricitabine (200mg) and tenofovir alafenamide (as fumarate) (10mg) fixed dose combination tablets、STRIBILD tenofovir disoproxil fumarate 300mg, emtricitabine 200 mg, elvitegravir 150 mg, cobicistat 150 mg tablet bottle
Records without a stated strength · 1 Genvoya、Stribild
US 2 records · 1 strengths
- 150 mgtabletGenvoyaStribild
CA 2 records · 1 strengths
- 150 mgtabletGenvoyaStribild
ES 2 records · 1 strengths
- 150 mgtabletGenvoyaStribild
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 Genvoya、Stribild
TW 1 records · 1 strengths
Records without a stated strength · 1 Genvoya、捷扶康 膜衣錠
| Strength / form / release | US | GB | CA | AU | ES | TW | EU |
|---|---|---|---|---|---|---|---|
| 150 mg tablet | Genvoya Stribild | Genvoya Stribild Vitekta 85mg tablets | Genvoya Stribild | Genvoya GENVOYA elvitegravir (150mg), cobicistat (150mg), emtricitabine (200mg) and tenofovir alafenamide (as fumarate) (10mg) fixed dose combination tablets STRIBILD tenofovir disoproxil fumarate 300mg, emtricitabine 200 mg, elvitegravir 150 mg, cobicistat 150 mg tablet bottle | Genvoya Stribild | ||
| 90 mg tablet | Genvoya | ||||||
| 85 mg tablet | Vitekta 85mg tablets | ||||||
unknown | Genvoya Stribild | Genvoya Stribild | |||||
tablet | Genvoya 捷扶康 膜衣錠 |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in TW and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en TW que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 TW 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 TW 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.
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.