FDA NDC Directory · JSON-LD · Markdown
NDC 65219-240 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION
| Generic name | Dextrose Monohydrate |
|---|---|
| Labeler / Manufacturer | Fresenius Kabi USA, LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA207449 |
| Dosage form / route | INJECTION, SOLUTION · INTRAVENOUS |
| Active ingredients | DEXTROSE MONOHYDRATE (25000 mg/500mL) |
| Marketing started | 20161021 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).