# OLPRUVA

NDC: 72542-600
Generic name: sodium phenylbutyrate
Labeler / Manufacturer: Acer Therapeutics Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: KIT
Routes: ORAL
Marketing started: 20221222

FDA application: NDA214860

## Active ingredients

—

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72542-600"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72542-600