Glycerol Phenylbutyrate
ATC A16AX09 · 6 markets · 15 records
US 10 records · 1 strengths
- 1,100 mgliquidGlycerol PhenylbutyrateRavicti、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 strengths
- 1,100 mgliquidRavicti 1.1g/ml oral
CA 1 records · 1 strengths
- 1,100 mgliquidRavicti
TW 1 records · 1 strengths
Records without a stated strength · 1 RAVICTI Oral Liquid、瑞維安口服液
HK 1 records · 1 strengths
Records without a stated strength · 1 RAVICTI ORAL LIQUID 1.1G/ML
EU 1 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 Ravicti
| Strength / form / release | US | GB | CA | TW | HK | EU |
|---|---|---|---|---|---|---|
| 1,100 mgRecorded as: 1.1 g liquid | Manufacturer: Aurobindo Pharma Limited Manufacturer: Lupin Pharmaceuticals, Inc. Manufacturer: Navinta LLC+6Manufacturer: 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 | |||
liquid | RAVICTI Oral 瑞維安口服液 | |||||
unknown | RAVICTI ORAL LIQUID 1.1G/ML | Ravicti |
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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.
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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.