FDA NDC Directory · JSON-LD · Markdown
NDC 63323-686 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION
| Generic name | Sodium Chloride and Potassium Chloride |
|---|---|
| Labeler / Manufacturer | Fresenius Kabi USA, LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA212347 |
| Dosage form / route | INJECTION, SOLUTION · INTRAVENOUS |
| Active ingredients | POTASSIUM CHLORIDE (150 mg/100mL) SODIUM CHLORIDE (900 mg/100mL) |
| Marketing started | 20210602 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).