Ammonul

Active Ingredient(s): Sodium Benzoate + Sodium Phenylacetate
FDA Approved: * February 17, 2005
Pharm Company: * UCYCLYD
Category: Hyperammonemia

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



Ammonul Overview

Sodium benzoate is a substance which has the chemical formula NaC7H5O2. It is a widely used food preservative, with an E number of E211. It is the sodium salt of benzoic acid and exists in this form when dissolved in water. It can be produced by reacting sodium hydroxide with benzoic acid. Contents 1 Production 2 Natural occurrence 3 Uses 3.1 Preservative 3.2 Pharmaceutical applications 3.3 Other uses 4 Mechanism of food preservation 5 Health and safety 5.1 Association with benzene in...

Read more Ammonul 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_benzoate

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Possible Dosages for this and Related Drugs:

Sodium Benzoate + Sodium Phenylacetate
  • Injection: 100mg/ml + 100mg/ml, 10ml + 50ml
  • Solution: 10% + 10%, 10% + 10% (5gm/50ml + 5gm/50ml), 100mg/ml + 100mg/ml
  • Solution, Solution: 300mg/10ml(30mg/ml),n/a + n/a,12.5gm/50ml(250mg/ml)
  • Tablet: 0.398gm + 1.102gm
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Ammonul: (2 results)

Sorted by National Drug Code
  • 0187-0010 Ammonul Intravenous Injection, Solution, Concentrate by Valeant Pharmaceuticals North America LLC
  • 62592-720 Ammonul Intravenous Injection, Solution, Concentrate by Ucyclyd Pharma Inc.

Drugs with one or more similar ingredients: (5 results)






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