Buphenyl

Active Ingredient(s): Sodium Phenylbutyrate
FDA Approved: * April 30, 1996
Pharm Company: * MEDICIS
Category: Hyperammonemia

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".



Buphenyl Overview

Sodium phenylbutyrate is a salt of an aromatic fatty acid, 4-phenylbutyrate (4-PBA) or 4-phenylbutyric acid.[1] The compound is used to treat urea cycle disorders, because its metabolites offer an alternative pathway to the urea cycle to allow excretion of excess nitrogen.[2][3] It is an orphan drug, marketed by Ucyclyd Pharma under the trade name Buphenyl, by Swedish Orphan International (Sweden) as Ammonaps, and by Fyrlklövern Scandinavia...

Read more Buphenyl Details
Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Sodium_phenylbutyrate

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Possible Dosages for this and Related Drugs:

Sodium Phenylbutyrate
  • Powder: 3g/tsp, 3gm/teaspoonful
  • Tablet: 500mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Buphenyl: (6 results)

Sorted by National Drug Code
  • 62592-188 Buphenyl .94 g/g Oral Powder by Ucyclyd Pharma Inc.
  • 62592-496 Buphenyl 500 mg Oral Tablet by Ucyclyd Pharma Inc.
  • 75987-060 Buphenyl 500 mg Oral Tablet by Horizon Pharma, Inc.
  • 75987-070 Buphenyl .94 g/g Oral Powder by Horizon Pharma, Inc.
  • 76325-188 Buphenyl .94 g/g Oral Powder by Hyperion Therapeutics, Inc.
  • 76325-496 Buphenyl 500 mg/1 Oral Tablet by Hyperion Therapeutics, Inc.

Other drugs which contain Sodium Phenylbutyrate or a similar ingredient: (1 result)






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