FDA NDC Directory · JSON-LD · Markdown
NDC 65219-243 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION
| Generic name | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, and DEXTROSE MONOHYDRATE |
|---|---|
| Labeler / Manufacturer | Fresenius Kabi USA, LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA210332 |
| Dosage form / route | INJECTION, SOLUTION · INTRAVENOUS |
| Active ingredients | CALCIUM CHLORIDE (20 mg/100mL) DEXTROSE MONOHYDRATE (5 g/100mL) POTASSIUM CHLORIDE (30 mg/100mL) SODIUM CHLORIDE (600 mg/100mL) SODIUM LACTATE (310 mg/100mL) |
| Marketing started | 20220328 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).