FDA NDC Directory · JSON-LD · Markdown
NDC 63323-669 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION
| Generic name | Potassium Chloride, Dextrose Monohydrate |
|---|---|
| Labeler / Manufacturer | Fresenius Kabi USA, LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA212346 |
| Dosage form / route | INJECTION, SOLUTION · INTRAVENOUS |
| Active ingredients | DEXTROSE MONOHYDRATE (5 g/100mL) POTASSIUM CHLORIDE (150 mg/100mL) |
| Marketing started | 20210423 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).