FDA NDC Directory · JSON-LD · Markdown
NDC 70511-102 · HUMAN PRESCRIPTION DRUG · INJECTION
| Labeler / Manufacturer | MAIA PHARMACEUTICALS |
|---|---|
| Marketing category | New Drug Application (innovator) · App NDA215025 |
| Dosage form / route | INJECTION · INTRAVENOUS |
| Active ingredients | SODIUM BENZOATE (100 mg/mL) SODIUM PHENYLACETATE (100 mg/mL) |
| Marketing started | 20210701 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).