Glycerol Phenylbutyrate

Records for this ingredient, by country (identity only).

ATC A16AX09 · 8 markets · 17 records

Glycerol Phenylbutyrate 8 markets · 17 records Forms

Filters

MarketUS 10 GB 1 CA 1 TW 1 HK 1 CZ 1 EU 1

Strength

US 10 records · 1 shown of 1 Source openFDA NDC Directory · Data as of 2026-10-23

1,100 mg per mL / per unit basis not statedliquidGlycerol Phenylbutyrate+8Ravicti、Manufacturer: Aurobindo Pharma Limited、Manufacturer: Lupin Pharmaceuticals, Inc.、Manufacturer: Navinta LLC、Manufacturer: Novadoz Pharmaceuticals LLC、Manufacturer: PAI Holdings, LLC dba PAI P…、Manufacturer: Teva Pharmaceuticals, Inc.、Manufacturer: Zydus Pharmaceuticals USA I…

GB 1 records · 1 shown of 1 Source NHSBSA dm+d · Data as of 2026-10-19

1,100 mg per mL / per unit basis not statedliquidRavicti 1.1g/ml oral

CA 1 records · 1 shown of 1 Source Health Canada Drug Product Databas · Data as of 2026-10-23

1,100 mg per mL / per unit basis not statedliquidRavicti

TW 1 records · 0 shown of 0 Source 衛生福利部食品藥物管理署（TFDA）全部藥品許可證資料集 · Data as of 2026-10-22 · some records have no stated strength

1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商

With a brand name Con nombre comercial 有商品名有商品名RAVICTI Oral Liquid ×1瑞維安口服液 ×1

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

HK 1 records · 0 shown of 0 Source 衞生署藥物辦公室（香港）註冊藥劑製品名單 · Data as of 2026-10-23 · some records have no stated strength · includes records with unknown status (not proof of sale)

1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商

With a brand name Con nombre comercial 有商品名有商品名RAVICTI ORAL LIQUID 1.1G/ML ×1

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

CZ 1 records · 1 shown of 1 Source Státní ústav pro kontrolu léčiv (S · Data as of 2026-11-01

1100 mg per mL / per unit basis not statedliquidRavicti

EU 1 records · 0 shown of 0 Source European Commission · Data as of 2026-11-03 · some records have no stated strength

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

With a brand name Con nombre comercial 有商品名有商品名Ravicti ×2

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

Some strengths are recorded without a per mL / per unit basis. They are shown as recorded and are not compared with other markets.

Side-by-side table

Strength / form / release	US	GB	CA	TW	HK	CZ	EU
1,100 mgRecorded as: 1.1 g per mL / per unit basis not stated cannot compare liquid	Manufacturer: Aurobindo Pharma Limited Manufacturer: Lupin Pharmaceuticals, Inc. Manufacturer: Navinta LLC +6 Manufacturer: Novadoz Pharmaceuticals LLC Manufacturer: PAI Holdings, LLC dba PAI P… Manufacturer: Teva Pharmaceuticals, Inc. Manufacturer: Zydus Pharmaceuticals USA I… Glycerol Phenylbutyrate Ravicti	Ravicti 1.1g/ml oral	Ravicti	not recorded	not recorded	not recorded	not recorded
1100 mgRecorded as: 1.1 g per mL / per unit basis not stated cannot compare liquid	not recorded	not recorded	not recorded	not recorded	not recorded	Ravicti	not recorded
not disclosed liquid	not recorded	not recorded	not recorded	RAVICTI Oral 瑞維安口服液	not recorded	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	not recorded	not recorded	RAVICTI ORAL LIQUID 1.1G/ML	not recorded	Ravicti

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

2 more strength/form rows are recorded only in HK · CZ · EU and are not shown in this table. Hay 2 filas de concentración/forma registradas solo en HK · CZ · EU que no se muestran en esta tabla. 另有 2 个规格/剂型仅在 HK · CZ · EU 有记录（未在本表显示）。另有 2 個規格/劑型僅在 HK · CZ · 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.

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.