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NDC 65219-151 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION
| Generic name | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE |
|---|---|
| Labeler / Manufacturer | Fresenius Kabi USA, LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA212348 |
| Dosage form / route | INJECTION, SOLUTION · INTRAVENOUS |
| Active ingredients | DEXTROSE MONOHYDRATE (50 g/1000mL) POTASSIUM CHLORIDE (1.49 g/1000mL) SODIUM CHLORIDE (2.25 g/1000mL) |
| Marketing started | 20220902 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).