Lopinavir

ATC J05AR · 10 markets · 50 records

Lopinavir 10 markets · 50 records Forms

US 9 records · 3 strengths

200 mgtabletKaletra+1__no_trade__ also in GB·AU·CA +3
100 mgtabletKaletra+1__no_trade__ also in GB·CA·ES
80 mgliquidKaletra also in SG

GB 7 records · 4 strengths

200 mgtabletKaletra+1__no_trade__ also in US·AU·CA +3
100 mgtabletKaletra also in US·CA·ES
400 mg/5 mLliquidKaletra also in AU
133.3 mgcapsuleKaletra

AU 5 records · 4 strengths

200 mgtabletKaletra+1KALETRA TABLETS lopinavir 200mg and ritonavir 50mg tablets bottle also in US·GB·CA +3 unknown
400 mg/5 mLliquidKaletra also in GB
80 mg/mLliquidKALETRA oral solution bottle unknown

Records without a stated strength · 1 Kaletra

HK 5 records · 1 strengths

Records without a stated strength · 1 Kaletra、LOPINAVIR AND RITONAVIR TABLETS USP 100MG/25MG

CA 3 records · 3 strengths

200 mgtabletKaletra also in US·GB·AU +3
100 mgtabletKaletra also in US·GB·ES
80 mg/1 mLliquidKaletra

ES 3 records · 3 strengths

200 mgtabletKaletra also in US·GB·AU +3
100 mgtabletKaletra also in US·GB·CA
400 mgliquidKALETRA MG)/ML

SG 2 records · 2 strengths

200 mgtabletKaletra also in US·GB·AU +3
80 mgliquidKaletra also in US

CN 2 records · 1 strengths

200 mgtablet克力芝洛匹那韦+1__mah__:安徽贝克生物制药有限公司 also in US·GB·AU +3

MX 2 records · 1 strengths

Records without a stated strength · 1 DALOVIA、GADANME

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 Kaletra、LOPINAVIR/RITONAVIR VIATRIS

Side-by-side table

Strength / form / release	US	GB	CA	AU	SG	CN	ES	MX	HK	EU
200 mg tablet	No trade name Kaletra	No trade name Kaletra	Kaletra	Kaletra KALETRA TABLETS lopinavir 200mg and ritonavir 50mg tablets bottle	Kaletra	Manufacturer: 安徽贝克生物制药有限公司克力芝洛匹那韦	Kaletra	not recorded	not recorded	not recorded
100 mg tablet	No trade name Kaletra	Kaletra	Kaletra	not recorded	not recorded	not recorded	Kaletra	not recorded	not recorded	not recorded
400 mg/5 mL liquid	not recorded	Kaletra	not recorded	Kaletra	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
80 mg liquid	Kaletra	not recorded	not recorded	not recorded	Kaletra	not recorded	not recorded	not recorded	not recorded	not recorded
133.3 mg capsule	not recorded	Kaletra	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
400 mg liquid	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	KALETRA MG)/ML	not recorded	not recorded	not recorded
80 mg/1 mL liquid	not recorded	not recorded	Kaletra	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
80 mg/mL liquid	not recorded	not recorded	not recorded	KALETRA oral solution bottle	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	not recorded	Kaletra	not recorded	not recorded	not recorded	not recorded	Kaletra LOPINAVIR AND RITONAVIR TABLETS USP 100MG/25MG	Kaletra LOPINAVIR/RITONAVIR VIATRIS
not disclosed tablet	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	DALOVIA GADANME	not recorded	not recorded

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Each country column shows the locally registered trade names — not translations.

3 more strength/form rows are recorded only in CA · ES · MX and are not shown in this table. Hay 3 filas de concentración/forma registradas solo en CA · ES · MX que no se muestran en esta tabla. 另有 3 个规格/剂型仅在 CA · ES · MX 有记录（未在本表显示）。另有 3 個規格/劑型僅在 CA · ES · 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.

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The same ingredient can carry completely different brand names in different countries, and the same name can point to a different ingredient. Listed by country — not interchangeable.

Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.