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NDC 76420-129 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION
| Generic name | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, and CALCIUM CHLORIDE |
|---|---|
| Labeler / Manufacturer | Asclemed USA, Inc. |
| Marketing category | New Drug Application (innovator) · App NDA017641 |
| Dosage form / route | INJECTION, SOLUTION · INTRAVENOUS |
| Active ingredients | CALCIUM CHLORIDE (20 mg/100mL) POTASSIUM CHLORIDE (30 mg/100mL) SODIUM CHLORIDE (600 mg/100mL) SODIUM LACTATE (310 mg/100mL) |
| Marketing started | 20190624 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).