Netarsudil
ATC S01EX05 · 7 markets · 14 records
US 2 records · 1 strengths
- 0.2 mgliquidRhopressaRocklatan
GB 2 records · 1 strengths
Records without a stated strength · 1 Roclanda 50micrograms/ml / 200micrograms/ml eye drops
SG 2 records · 1 strengths
Records without a stated strength · 1 RHOPRESSA OPHTHALMIC SOLUTION, 0.02% w/v、ROCKLATAN OPHTHALMIC SOLUTION, 0.02% W/V / 0.005% W/V
ES 2 records · 1 strengths
- 0.2 mg/1 mLliquidROCLANDA
HK 2 records · 1 strengths
Records without a stated strength · 1 RHOPRESSA EYE DROPS 0.02% W/V、ROCKLATAN EYE DROPS
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 Rhokiinsa、ROCLANDA
TW 1 records · 1 strengths
Records without a stated strength · 1 Rocklatan 0.05 mg/ml + 0.2 mg/ml, eye drops, solution、絡可坦點眼液
| Strength / form / release | US | GB | SG | ES | TW | HK | EU |
|---|---|---|---|---|---|---|---|
| 0.2 mg liquid | Rhopressa Rocklatan | ||||||
| 0.2 mg/1 mLRecorded as: 200 mcg/1 mL liquid | ROCLANDA | ||||||
liquid | Roclanda 50micrograms/ml / 200micrograms/ml eye drops | RHOPRESSA OPHTHALMIC SOLUTION, 0.02% w/v ROCKLATAN OPHTHALMIC SOLUTION, 0.02% W/V / 0.005% W/V | Rocklatan 0.05 mg/ml + 0.2 mg/ml, eye drops, solution 絡可坦點眼液 | ||||
unknown | RHOPRESSA EYE DROPS 0.02% W/V ROCKLATAN EYE DROPS | Rhokiinsa ROCLANDA |
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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.
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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.