FDA NDC Directory · JSON-LD · Markdown
NDC 73352-905 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION
| Labeler / Manufacturer | Trifluent Pharma, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA217914 |
| Dosage form / route | POWDER, FOR SOLUTION · ORAL |
| Active ingredients | LACTULOSE (20 g/20g) |
| Marketing started | 20250913 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).