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Drug profile · INN

sodium phenylbutyrate

AMMONAPS

approved A16AX03
US status
approved
Patents linked
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News articles
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Quick answer

sodium phenylbutyrate (AMMONAPS) is an FDA-listed pharmaceutical active ingredient. Associated with Amylyx Pharmaceuticals EMEA B.V.. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN sodium phenylbutyrate
Brand AMMONAPS
Route ORAL
Formulation FOR SUSPENSION
ATC code A16AX03

Frequently asked questions

What is sodium phenylbutyrate?

sodium phenylbutyrate (AMMONAPS) is an FDA-listed pharmaceutical active ingredient. Associated with Amylyx Pharmaceuticals EMEA B.V.. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for sodium phenylbutyrate?

AMMONAPS is a marketed brand name for sodium phenylbutyrate. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of sodium phenylbutyrate?

sodium phenylbutyrate has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.