FDA NDC Directory · JSON-LD · Markdown
NDC 0121-1049 · HUMAN PRESCRIPTION DRUG · LIQUID
| Labeler / Manufacturer | PAI Holdings, LLC dba PAI Pharma |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA220579 |
| Dosage form / route | LIQUID · ORAL |
| Active ingredients | GLYCEROL PHENYLBUTYRATE (1.1 g/mL) |
| Marketing started | 20261012 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).